Restenosis/atherosclerosis diagnosis, prophylaxis and therapy

ABSTRACT

Disclosed and claimed are compositions and methods for therapy and/or prevention of restenosis and/or atherosclerosis. The compositions can include an agent for decreasing viral load of cytomegalovirus, such as an immunological composition or vaccine against cytomegalovirus (CMV) containing at least one epitope of interest of CMV and/or an expression system which expresses at least one epitope of interest of CMV. Such compositions can include at least one epitope of p53. Alternatively, the compositions can include at least one epitope of p53 and/or an expression system which expresses the epitope. The methods can include administering the compositions to a patient in need of such therapy and/or prevention. Additionally, compositions and methods for diagnosing atherosclerosis and/or restenosis, or susceptibility thereto, including screening a sample from a patient for antibodies to CMV and/or CMV proteins and/or screening a sample from a patient for specific viral proteins that predict whether the virus has been reactivated and/or antibodies thereto and/or detecting whether CMV nucleic acid, e.g., mRNA is present in peripheral blood monocytes (PBMCs) and/or detecting a cellular-mediated immune response to CMV peptides or proteins is present and/or HLA phenotyping and/or HLA genotyping. Embodiements can include a skin test.

FIELD OF THE INVENTION

The present invention relates to compositions and methods for the diagnosis, prophylaxis and/or therapy of restenosis and/or atherosclerosis.

The present invention relates to the use of an agent for decreasing viral load, e.g., an immunological composition, preferably a vaccine, against cytomegalovirus and/or p53 for therapy for restenosis and/or atherosclerosis; and, to a method for providing therapy for restenosis and/or atherosclerosis comprising administering the agent for decreasing viral load, e.g., an immunological composition or vaccine, against cytomegalovirus (CMV) and/or p53.

“Viral load” and “virus load”, as used herein, can have their art-recognized definitions, and can refer to active virus, e.g. virus in circulation or infectious, non-dormant virus, as well as virus which is latent or dormant awaiting reactivation or reactivating, or virus which is having an abortive replication cycle. While restenosing patients may not have any increase in IgG or IgM, Applicants, without wishing to necessarily be bound by any one particular theory, submit that viral reactivation following angioplasty/atherectomy can occur; and, that this viral reactivation, in some instances, may only proceed as far as the turn-on of IE genes and not up to viremia. Thus, “viral activation” is included in “viral load” and “virus load” herein. Further, “atherectomy” is included in “angioplasty” herein.

The CMV antigen can derive from any CMV protein, including immediate early (IE), early, or late gene products. The antigen can be the entire protein or an antigenic portion thereof.

The p53 can be wild-type or a mutant, e.g., full-length p53 or a truncated antigenic portion thereof.

The antigen(s) can be derived recombinantly, e.g., from expression by a virus, bacteria, or plasmid, in vitro, with subsequent isolation and purification; or from expression by a recombinant in vivo. Preferred expression systems include generally adenovirus, baculovirus, poxvirus, and DNA vector systems. For in vivo use, a recombinant adenovirus or poxvirus, such as a vaccinia virus or avipox virus (e.g., canarypox virus), or a DNA vector system are preferred; but, any suitable vector system, including naked DNA, may be employed. Indeed, as herpesvirus vectors are known, a replication-deficient herpesvirus vector, e.g., a replication-defective HSV or CMV vector could even be used in embodiments of the invention.

The invention thus relates to stimulating an immune response, preferably a cellular immune response, directed against CMV and/or p53 to inhibit or prevent restenosis and/or atherosclerosis and/or smooth muscle proliferation. Such a response can cause cell lysis and thus inhibition of smooth muscle cell proliferation and/or inhibition of atherosclerosis and/or restenosis. Thus, the invention relates to methods for inducing cell lysis of smooth muscle cells and/or inhibition of smooth muscle cell proliferation to treat or prevent restenosis and/or atherosclerosis.

The administration of the immunological composition or vaccine can be before or at the time of angioplasty, e.g., coronary and/or peripheral angioplasty, to prevent the development of restenosis, or independently of angioplasty, to provide treatment for atherosclerosis. It can also be administered any time during the lifetime of the individual, from childhood to adulthood, to prevent the development or progression of atherosclerosis. Thus, the invention relates to a therapeutic method for treatment of atherosclerosis and/or restenosis.

The immunological composition or vaccine can be administered alone or with additional therapeutic treatment; and, the invention further relates to additional methods for therapeutic treatment of restenosis and/or atherosclerosis.

The additional therapeutic treatment can comprise therapy for decreasing viral burden, e.g., the administration of: antioxidants which inhibit the replication of CMV and the cytopathic effect of viral infection, and/or compositions which reduce the transcriptional activity of CMV (transcriptional activity reducer) and/or compositions which decrease reactive oxygen species (ROS) generated by the arachidonic cascade and/or the xanthine/xanthine oxidase system (ROS reducer). Additionally or alternatively, the additional therapeutic treatment can comprise administration of an antiviral agent such as gancyclovir and/or acyclovir.

Thus, the invention still further relates to a method for treatment of atherosclerosis and/or restenosis comprising administering a sufficient dose or doses of at least one agent for decreasing viral burden and/or directed to interfering with SMC proliferation, e.g., antioxidant which inhibits the cytopathic effect of viral infection and/or transcriptional activity reducer and/or ROS reducer, either alone, or in conjunction with the aforementioned immunological composition or vaccine therapy.

The antioxidant can be one or more of Vitamin C, Vitamin E, NAC, PDTC, and the like.

The transcriptional activity reducer can be an antiviral drug such as gancyclovir and/or acyclovir (which interfere with viral replication), and/or an antioxidant, or the like.

The ROS reducer can be aspirin (acetylsalicylic acid) or a derivative thereof, ASA, Indomethacin, oxypurinol, and the like.

Accordingly, the invention additionally relates to a method for treating restenosis and/or atherosclerosis comprising, after angioplasty: administering a sufficient dose or doses of an immunological composition, preferably a vaccine, against CMV and/or p53; or administering a sufficient dose or doses of an immunological composition, preferably a vaccine, against CMV and/or p53, with or without a sufficient dose or doses of an antioxidant which inhibits viral infection and/or the cytopathic effect of viral infection and/or transcriptional activity reducer and/or ROS reducer; or administering a sufficient dose or doses of one or more antioxidant which inhibits viral replication and/or the cytopathic effect of viral infection and/or transcriptional activity reducer and/or ROS reducer.

The compositions administered after angioplasty can be used before angioplasty, to prevent, i.e., as a prophylaxis against, restenosis and/or atherosclerosis.

Accordingly, the invention relates to a method for preventing restenosis and/or atherosclerosis comprising, before angioplasty: administering a sufficient dose or doses of an immunological composition, preferably a vaccine, against CMV and/or p53; or administering a sufficient dose or doses of an immunological composition, preferably a vaccine, against CMV and/or p53 with or without a sufficient dose or doses of at least one composition for decreasing viral burden and/or directed to interfering with SMC proliferation, e.g., antioxidant which inhibits the cytopathic effect of viral infection and/or transcriptional activity reducer and/or ROS reducer; or administering a sufficient dose or doses of at least one agent for decreasing viral burden and/or directed to interfering with SMC proliferation, e.g., antioxidant which inhibits the cytopathic effect of viral infection and/or transcriptional activity reducer and/or ROS reducer. Thus, the invention can relate to treatment or prophylaxis directed at both decreasing viral loads, and decreasing SMC proliferation.

Interesting therapeutic or prophylactic compositions and methods of the invention relate to recombinants, especially for in vivo use, expressing a CMV antigen or portion thereof, or p53 or a portion thereof, or a combination of a CMV antigen or portion thereof and p53 or a portion thereof. These recombinants can additionally express or be used in conjunction with another form of molecular based therapy, e.g., expression of cytotoxic molecules to inhibit proliferation of smooth muscle cells, gene therapy, or antisense strategies to inhibit expression of gene products for cell proliferation. Thus, an embodiment can be providing treatment directed at decreasing viral load and treatment directed at reducing SMC proliferation.

Accordingly in certain aspects, the present invention relates to vaccine or immunological compositions for treatment or prophylaxis of restenosis and/or atherosclerosis, including compositions containing a CMV antigen or portion thereof, e.g., IE1, IE2, IE1 and IE2, or antigenic portions thereof or any other CMV antigens from IE, early, or late gene products, p53 or an antigenic portion thereof, or a CMV antigen or portion thereof and p53 or portion thereof. The present invention can include compositions containing naked DNA expressing the CMV antigen or protion thereof, or a recombinant or recombinants expressing the CMV antigen or portion thereof and/or p53 or an antigenic portion thereof or such an antigen or portion thereof from recombinant expression. The present invention further includes uses of such compositions with additional treatment or therapy, including compositions containing a recombinant or recombinants expressing a component of such additional treatment or therapy or co-expressing the component of such additional treatment or therapy with the CMV antigen or portion thereof and/or p53 or an antigenic portion thereof, and methods of making and using such compositions. Naked DNA or recombinants used in the present invention can be of varied type; for instance, one antigen or portion thereof or component of additional therapy may be expressed in one type of system, and another antigen or portion thereof or component of additional therapy (if present) may be from the same, or a different, system.

The method for diagnosis to ascertain a susceptibility to atherosclerosis and/or restenosis can comprise immunologically detecting CMV antibodies, either against the whole or any part of the virus, or preferably against specific viral proteins that more specifically reflect reactivation of the virus such as IE72, IE84, IE55 and the like. The immunologically detecting can be by ELISA and/or immunoblotting. Alternatively, detection can be for the CMV antigen.

The method can include, in addition or alternatively to detecting the neutralizing antibodies or antigens elicited thereby, detecting whether CMV mRNA is present in peripheral blood monocytes (PBMCs), e.g., by PCR (such as RT-PCR) and/or detecting whether a cellular-mediated immune response to CMV peptides or proteins is present, e.g., whether PBMCs recognize and/or respond to CMV peptides or proteins.

This aspect of the invention can relate to a skin test whereby the CMV proteins or peptides are administered subcutaneously or intradermally or intramuscularly, which reflects the patient's capacity to mount a cellular-mediated response targeted to the CMV proteins or peptides. A negative vs. a positive skin test for patients with prior CMV infection reflects the capacity to not develop, or to develop, respectively, a cell-mediated immune response to CMV. Such a test allows a prediction of who is susceptible and who is resistant to atherosclerosis and/or restenosis.

This aspect of the invention can relate more generally to presenting the patient's PBMCs with CMV proteins or peptides and measuring either the proliferative response of the cells or the cytokine profile to determine whether there is a dominant Th1 (e.g., IL-2, IFN-12, IFNγ) or Th2 (IL-4, IL-10) response.

This aspect of the invention can also relate to HLA phenotyping and/or HLA genotyping, as such phenotyping and/or genotyping can be used to predict the susceptibility to CMV-induced vascular disease.

This aspect of the invention can further relate to detection of p53. CMV interacts with p53 in smooth muscle cells (SMCs). p53 present in increased amounts binds to MHC Class I antigens in the SMCs and is processed and presented at the cell surface at an increased rate, resulting in stimulation of T cell response, underlying the antibody responses (whereas normal p53 is immunologically silent). Increased or steady state levels of p53 are present in cancers or when viral oncoproteins bind to p53 (as is the case with CMV).

Thus, the diagnostic method can comprise screening a sample from a patient (e.g., sera, blood, SMCs, etc.) for antibodies to CMV. The method can further comprise: screening a sample from a patient for specific viral proteins or antibodies thereto that are more specific predictors of whether the virus has been reactivated such as IE72, IE84, IE55 and the like; and/or detecting whether CMV mRNA is present in PBMCs, e.g., by PCR (such as RT-PCR); and/or detecting whether a cellular-mediated immune response to CMV peptides or proteins is present, e.g., whether PBMCs recognize and/or respond to CMV peptides or proteins, e.g., by administering a CMV skin test by administering CMV proteins or peptides intradermally or subcutaneously or intramuscularly and ascertaining the result of the skin test and/or presenting CMV proteins or peptides to a patient's PBMCs and measuring either the proliferative response of the cells (PMBCs) or the cytokine profile; and/or HLA phenotyping and/or HLA genotyping; and optionally screening a sample from a patient (e.g., sera, blood, SMCS, lesions,) for p53.

The initial screening for antibodies to CMV may optionally be omitted, such that the diagnostic method can comprise: screening a sample from a patient for specific viral proteins that predict whether the virus has been reactivated such as IE72, IE84, IE55 and the like; and/or detecting whether CMV mRNA is present in PBMCs, e.g., by PCR (such as RT-PCR); and/or detecting whether a cellular-mediated immune response to CMV peptides or proteins is present, e.g., whether PBMCs recognize and/or respond to CMV peptides or proteins, e.g., by administering a CMV skin test by administering CMV proteins or peptides intradermally or subcutaneously or intramuscularly and ascertaining the result of the skin test and/or presenting CMV proteins or peptides to a patient's PBMCs and measuring either the proliferative response of the cells (PMBCs) or the cytokine profile; and/or HLA phenotyping and/or HLA genotyping; and optionally screening a sample from a patient (e.g., sera, blood, SMCs, lesions, etc.) for p53.

The diagnostic method of the invention can also be used to test for stratification of atherosclerosis and/or restenosis risk factors.

The CMV proteins or peptides can be purified CMV proteins or peptides from lysates of cells previously infected with CMV, or from recombinant expression of the CMV proteins or peptides. Antibodies to such may also be used in diagnostic and therapeutic and/or preventative composition and methods of the invention. And, the CMV in the various aspects to which the invention pertains can be of any suitable cytomegalovirus, including, human CMV (HCMV) murine CMV (MCMV) or rat CMV (RCMV) origin, with HCMV and RCMV embodiments preferred.

Various documents are cited in the following text, or in a reference section preceding the claims. Each of the documents cited herein, and each of the references cited in each of those various documents, is hereby incorporated herein by reference. None of the documents cited in the following text is admitted to be prior art with respect to the present invention.

BACKGROUND OF THE INVENTION

As discussed generally by Jean Marx at page 320 of Science, Vol. 265 (Jul. 15, 1994), each year about 330,000 patients in the United States undergo coronary and/or peripheral angioplasty, a procedure designed to open up blood vessels, e.g., coronary arteries, clogged by dangerous atherosclerotic plaques (atherosclerosis) and thereby restore normal blood flow. For a majority of these patients, the operation works as intended. Nearly 33% of these patients (and maybe more by some accounts), however, develop restenosis, wherein the treated arteries become quickly clogged again. These patients are no better off, and sometimes worse off, than they were before angioplasty. Excessive proliferation of smooth muscle cells in blood vessel walls contributes to restenosis.

Improvements in the therapy, prophylaxis and diagnosis of restenosis and/or atherosclerosis, especially in compositions therefore and methods thereof, would be an advance over the state of the art.

In 1950, Patterson and Cottral, in Arch. Pathol. 1950; 49:699, called attention to the development of coronary atherosclerosis in chickens ill with Marek's lymphomatosis, the etiological agent of which was subsequently discovered to be a herpesvirus now known as Marek's Disease Virus.

Melnick et al. in European Heart Journal (1993) 14 (Supplement K), 30-38, and BioEssays Vol. 17, No. 10 pp. 899-903 (1995) report that the finding in chickens prompted studies of human herpesviruses with respect to human atherosclerosis.

In Melnick et al., European Heart Journal, supra, circumstantial evidence for involvement of CMV is presented. This evidence includes finding CMV antigen and nucleic acid sequences in arterial smooth muscle cells of humans, seroepidemiological studies showing high levels of CMV antibodies found associated with clinically manifest atherosclerotic disease, suggesting that a periodically activated latent infection or a continuously active infection is present in patients with atherosclerosis. However, the viral genome, but not the infectious virus, was found in arterial cells, leading the authors to assert that the artery itself may be the site of CMV latency. The authors caution that their observations do not demonstrate that viruses have a role in the pathogenesis of atherosclerosis.

In Melnick et al., BioEssays, supra, the authors report that antigens and nucleic acid sequences of CMV, a widespread member of the herpesvirus family, were found in arterial lesions in human atherosclerosis; but, infectious virus has not been observed. In atherosclerosis patients, high levels of CMV antibodies are present, suggesting the presence of virus that had been activated from a latent state.

There is no teaching or suggestion in Melnick et al., BioEssays, supra, of any particular CMV vaccine or any particular strategy for treatment, prevention or diagnosis of restenosis or atherosclerosis.

Speir et al., Science 265:391-394 (Jul. 15, 1994) postulate that restenosis may be triggered by activation of latent CMV, e.g., by angioplasty-induced injury to the vessel wall, that causes multiple cellular changes and predispose SMCs to proliferate. For instance, Speir et al. postulate that CMV protein IE84 combines with and inactivates p53 in smooth muscle cells, which, in turn could predispose the cells towards increased growth, analogous to the way p53 inactivation is believed to contribute to the formation of malignant tumors. This CMV-mediated inhibition of p53, assert Speir et al., may in part explain the monoclonality observed in some atherosclerotic lesions (see Benditt and Benditt, PNAS USA 70: 1753 (1973)).

As Jean Marx, supra, observed, the Speir et al. hypothesis is just one of many potential mechanisms by which the virus may produce restenotic lesions. Jean Marx, supra, further observed that CMV activation cannot explain all cases of restenosis, as signs of a CMV-p53 interaction have not been found in about 67% of the restenosis samples.

Golubev et al., U.S. Pat. No. 5,534,258 (not admitted to be prior art), relates to four polypeptides from certain herpesviruses; specifically two polypeptides from HSV-1, and two polypeptides from CMV. Golubev et al., without any data, speculates that this shotgun approach of a combination of all four of these polypeptides, in equal proportion, is a prophylactic vaccine against pathogenic development of atherosclerotic plaque. No protection data is presented.

Literature involving CMV and/or restenosis and/or atherosclerosis, as discussed above likewise fails to teach or suggest any therapy or prophylaxis or any detection methods, or any compositions therefor, for restenosis and/or atherosclerosis, as in the present invention. Indeed, heretofore there had not been a definitive teaching or suggestion in the art of a relation between the presence of antibodies to CMV at the time of angioplasty, indicating prior exposure to CMV, and the subsequent development of restenosis. And, even if, assuming arguendo (with no admission), one asserted some sort of teaching or suggestion of any relation between CMV or antibodies thereto and restenosis and/or atherosclerosis, there is still a failure to teach or suggest any therapy or prophylaxis or any detection methods, or any compositions therefor, for restenosis and/or atherosclerosis, as in the present invention.

It would indeed be an advance in the art to show a connection between CMV and restenosis and/or atherosclerosis, especially mechanisms involving the virus, including such as the virus, by inhibiting either the capacity of p53 to block cell cycle progression, or its capacity to initiate apoptosis, enhances SMC accumulation and thereby facilitates development of restenotic lesions, as herein.

Indeed, it is believed that heretofore there has been no evidence linking viremia and angioplasty, such as balloon angioplasty, and subsequent restenosis in humans, e.g., no boost of immune response, such that there is a fortiori no teaching or suggestion of any prophylaxis or treatment for restenosis and/or atherosclerosis or compositions therefor or methods for making such compositions.

OBJECTS AND SUMMARY OF THE INVENTION

It is therefore an object of the invention to provide methods and compositions for the diagnosis of, prophylaxis of and/or therapy for restenosis and/or atherosclerosis.

It is yet a further object of the invention to provide such methods and compositions for prophylaxis and/or therapy which comprise an agent for decreasing viral load, e.g., a vaccine or immunological compositions.

It is a still further object of the invention to provide such methods and compositions including gene products from in vitro and/or in vivo expression from plasmid DNA, or a vector system, such as a recombinant viral and/or DNA expression system.

It is yet another object to provide such methods and compositions wherein the gene products comprise a CMV antigen, e.g., IE1 and/or IE2 or a portion thereof; gB; gB with transmembrane deleted therefrom; gH; gL; pp150; pp65; IE1 with amino acids 2-32 deleted therefrom; IE1 with amino acids 292-319 deleted therefrom; IE1 exon 4 segment; gB and gH; gB and pp65; gB, gH and pp65; gB, gH, pp65 and IE1 exon 4 segment; gB, gH, pp65, pp150, and IE1 exon 4 segment; gB, gH, pp65 and pp150; gB, gH, gL, pp65, pp150and IE1 exon 4 segment; and gB, gH, gL, pp65 and pp150; gp64; or portion of such CMV antigens; or p53 or a portion thereof, or a CMV antigen or portion thereof and p53 or a portion thereof; and, such a portion thereof can be an antigenic portion; for instance, an epitope of interest.

It is a yet further object of the invention to provide such methods and compositions in conjunction with additional treatment methods and compositions.

It is another object of the invention to provide diagnostic methods and compositions.

It is a further object of the invention to provide such diagnostic methods and compositions, including screening a sample from a patient for specific viral proteins or antibodies thereto that predict whether the virus has been reactivated such as IE72, IE84, IE55 and the like; and/or detecting whether CMV nucleic acid such as mRNA is present in PBMCs, e.g., by PCR (such as RT-PCR); and/or detecting whether a cellular-mediated immune response to CMV peptides or proteins is present, e.g., whether PBMCs recognize and/or respond to CMV peptides or proteins, e.g., by administering a CMV skin test by administering CMV proteins or peptides intradermally or subcutaneously or intramuscularly and ascertaining the result of the skin test and/or presenting CMV proteins or peptides to a patient's PBMCs and measuring either the proliferative response of the cells (PMBCs) or the cytokine profile; and/or HLA phenotyping and/or HLA genotyping; and optionally screening a sample from a patient (e.g., sera, blood, SMCs, lesions, etc.) for p53; with optional initial screening for antibodies to CMV, which may optionally be omitted.

It is yet another object of the invention to demonstrate a relation between the presence of antibodies to CMV at the time of angioplasty, indicating prior exposure to CMV, and the subsequent development of restenosis.

It is a still further object of the invention to provide compositions and methods arising as a consequence of demonstrating that there is such a relation.

It is still another object of the invention to show a connection between CMV and restenosis and/or atherosclerosis, especially mechanisms involving the virus, including such as the virus, by inhibiting either the capacity of p53 to block cell cycle progression, or its capacity to initiate apoptosis, enhances SMC accumulation and thereby facilitates development of restenotic lesions.

It is even a still further object of the invention to provide compositions and methods arising as a consequence of demonstrating that there is such a connection and/or mechanisms.

The present invention thus provides methods and compositions for the diagnosis of, prophylaxis of and/or therapy for restenosis and/or atherosclerosis.

The present invention further provides such methods and compositions for prophylaxis and/or therapy which comprise compositions for decreasing viral burden, e.g., vaccine or immunological compositions.

The present invention also provides such methods and compositions including gene products from in vitro and/or in vivo expression from plasmid DNA, a vector system, such as a recombinant viral or DNA expression system.

The present invention additionally provides such methods and compositions wherein the gene products comprise a CMV antigen, e.g., IE1 and/or IE2, or other viral gene products or portion thereof, or p53 or a portion thereof, or a CMV antigen or portion thereof and p53 or a portion thereof; and, such a portion thereof can be an antigenic portion; for instance, an epitope of interest.

The present invention even further provides such methods and compositions in conjunction with additional treatment methods and compositions.

The present invention thus provides an immunological composition, preferably a vaccine, against cytomegalovirus and/or p53 for therapy for restenosis and/or atherosclerosis; and, a method for providing therapy for restenosis and/or atherosclerosis comprising administering the immunological composition or vaccine against cytomegalovirus (CMV) and/or p53.

The CMV antigen can be IE1 or an antigenic portion thereof, IE2 or an antigenic portion thereof, or, or another CMV gene product or an antigenic portion thereof, wherein the antigenic portion can be an epitope of interest; and, can be of any suitable origin, e.g., human CMV, murine CMV or rat CMV origin, with human CMV (HCMV) preferred.

The p53 can be wild-type or a mutant, e.g., full-length p53 or a truncated antigenic portion thereof; again, wherein the antigenic portion can be an epitope of interest.

The antigen(s) can be derived recombinantly, e.g., from expression by a virus, bacteria, or plasmid, in vitro, with subsequent isolation and purification; or from expression by a recombinant or plasmid in vivo. Preferred vector systems include plasmid DNA, adenovirus, baculovirus, poxvirus, and DNA expression systems. For in vivo use, plasmid DNA, a recombinant adenovirus or poxvirus, such as a vaccinia virus or avipox virus (e.g., canarypox virus), or a DNA expression system are preferred; but, any suitable vector system, including may be employed. Thus, as herpesvirus vectors are known, a replication-deficient herpesvirus vector, e.g., a replication-defective HSV or CMV vector could even be used in embodiments of the invention.

The invention thus provides compositions and methods for stimulating an immune response, preferably a cellular immune response, directed against CMV and/or p53 to inhibit or prevent restenosis and/or atherosclerosis and/or smooth muscle proliferation. Such a response can cause lysis of infected cells thereby eliminating virus or reducing virus load, and thus inhibit smooth muscle cell proliferation and/or restenosis and/or atherosclerosis. Thus, the invention provides methods and compositions for inducing cell lysis of infected smooth muscle cells and/or inhibition of smooth muscle cell proliferation to treat or prevent restenosis and/or atherosclerosis.

The administration of the immunological composition or vaccine can be after angioplasty, coronary and/or peripheral angioplasty, to prevent the development of, or to provide treatment for, atherosclerosis and/or restenosis. Thus, the invention provides a therapeutic method for treatment of atherosclerosis and/or restenosis, and compositions therefor.

The immunological composition or vaccine can be administered alone or with additional therapeutic treatment; and, the invention further provides additional methods and compositions for therapeutic treatment of restenosis and/or atherosclerosis.

The additional therapeutic treatment can comprise the administration of: antioxidants which inhibit the cytopathic effect of viral infection, and/or compositions which reduce the transcriptional activity of CMV (transcriptional activity reducer) and/or compositions which decrease reactive oxygen species (ROS) generated by the arachidonic cascade and/or the xanthine/xanthine oxidase system (ROS reducer).

Thus, the invention still further provides to a method for treatment of atherosclerosis and/or restenosis comprising administering a sufficient dose or doses of at least one antioxidant which inhibits the cytopathic effect of viral infection and/or transcriptional activity reducer and/or ROS reducer, either alone, or in conjunction with the aforementioned immunological composition or vaccine therapy; and, the invention provides such compositions.

The antioxidant can be one or more of Vitamin C, Vitamin E, NAC, PDTC, and the like.

The transcriptional activity reducer can be an antiviral drug such as gancyclovir and/or acyclovir (which interfere with viral replication), and/or an antioxidant, or the like.

The ROS reducer can be aspirin (acetylsalicylic acid) or a derivative thereof, ASA, oxypurinol, and the like.

Accordingly, the invention additionally provides a method for treating restenosis and/or atherosclerosis comprising, before, during or after angioplasty, or at any time during the lifetime of the individual, from childhood to adulthood, to prevent the development or progression of atherosclerosis: administering a sufficient dose or doses of an immunological composition, preferably a vaccine, against CMV and/or p53; or administering a sufficient dose or doses of an immunological composition, preferably a vaccine, against CMV and/or p53 in conjunction with a sufficient dose or doses of at least one antioxidant which inhibits replication and the cytopathic effect of viral infection and/or transcriptional activity reducer and/or ROS reducer; or administering a sufficient dose or doses of at least one antioxidant which inhibits replication and the cytopathic effect of viral infection and/or transcriptional activity reducer and/or ROS reducer. And, the invention provides compositions for these methods.

The compositions are administered before, during, or after angioplasty; before angioplasty, to prevent, i.e., as a prophylaxis against, restenosis and/or atherosclerosis. They can also be administered any time during the lifetime of the individual, from childhood to adulthood, to prevent the development or progression of atherosclerosis.

Accordingly, the invention provides a method for preventing restenosis and/or atherosclerosis comprising, before, during, or after angioplasty to prevent, e.g., as a prophylaxis against restenosis and/or atherosclerosis, or at any time during the lifetime of the individual, from childhood to adulthood, to prevent the development or progression of atherosclerosis: administering a sufficient dose or doses of an immunological composition, preferably a vaccine, against CMV and/or p53; or administering a sufficient dose or doses of an immunological composition, preferably a vaccine, against CMV and/or p53 in conjunction with a sufficient dose or doses of at least one antioxidant which inhibits the cytopathic effect of viral infection and/or transcriptional activity reducer and/or ROS reducer; or administering a sufficient dose or doses of at least one antioxidant which inhibits the cytopathic effect of viral infection and/or transcriptional activity reducer and/or ROS reducer. And, the invention provides compositions for these methods.

The invention further provides therapeutic or prophylactic compositions and methods of the invention relating to plasmid DNA or recombinants, especially for in vivo use, expressing a CMV antigen or portion thereof, or p53 or a portion thereof, or a combination of a CMV antigen or portion thereof and p53 or a portion thereof; and, these recombinants can additionally express or be used in conjunction with another form of molecular based therapy, e.g., expression of cytotoxic molecules to proliferating smooth muscle cells, gene therapy, or antisense strategies to inhibit expression of gene products for cell proliferation. The invention can provide compositions and methods directed at reducing viral load and inhibiting SMC proliferation.

Accordingly in certain aspects, the present invention provides vaccine or immunological compositions for treatment or prophylaxis of restenosis and/or atherosclerosis, including compositions containing a CMV antigen or portion thereof, e.g., IE1, IE2, IE2 and IE2, or antigenic portions thereof, p53 or an antigen portion thereof, a CMV antigen or portion thereof and p53 or portion thereof, such as compositions containing a recombinant or recombinants expressing the CMV antigen or portion thereof and/or p53 or antigenic portion thereof or such an antigen or portion thereof from recombinant expression, uses of such compositions with additional treatment or therapy, including compositions containing a recombinant or recombinants expressing a component of such additional treatment or therapy or co-expressing the component of such additional treatment or therapy with the CMV antigen or portion thereof and/or p53 or antigenic portion thereof, and methods of making and using such compositions (wherein a portion of an antigen can be an epitope of interest).

Recombinants used in the present invention can be of varied type; for instance, one antigen or portion thereof or component of additional therapy may be expressed in one type of system, and another antigen or portion thereof or component of additional therapy (if present) may be from the same, or a different, system.

Plasmid DNA or recombinants of the present invention can have in vivo expression at any suitable level for treatment and/or prophylaxis of restenosis and/or atherosclerosis, which can be determined by the skilled artisan without undue experimentation.

Recombinants can be administered in an amount of about 10⁷ pfu; thus, the inventive compositions can contain, and the inventive methods involve, administering a composition containing recombinant(s), at least this amount; more preferably about 10⁴ pfu to about 10¹⁰ pfu, e.g., about 10⁵ pfu to about 10⁹ pfu, for instance about 10⁶ pfu to about ₁₀ ⁸ pfu. And, if more than one gene product is expressed by more than one recombinant, each recombinant can be administered in these amounts; or, each recombinant can be administered such that there is, in combination, a sum of recombinants comprising these amounts.

In naked DNA and DNA plasmid compositions, the dosage should be a sufficient amount of naked DNA or DNA plasmid to elicit a response analogous to the expressed antigen compositions; or expression analogous to dosages in expressed antigen compositions; or expression analogous to expression obtained in vivo by other, e.g., viral, recombinant compositions. For instance, suitable quantities of naked DNA or plasmid DNA in naked DNA or DNA plasmid compositions can be 1 ug to 100 mg, preferably 0.1 to 10 mg, but lower levels such as 0.1 to 2 mg or even 1-10 ug, may be employed.

And, if more than one gene product is expressed by more than one recombinant and/or DNA (naked or plasmid) system, each recombinant and/or DNA system can be administered in these amounts; or, each recombinant and/or DNA system can be administered such that there is, in combination, a sum of recombinants and/or DNA comprising these amounts.

Subcutaneous, intradermal or intramuscular administration are presently preferred.

The present invention includes diagnostic methods and compositions.

The present invention also provides such diagnostic methods and compositions, including screening a sample from a patient for specific viral proteins or antibodies thereto that predict whether the virus has been reactivated such as IE72, IE84, IE55 and the like; and/or detecting whether CMV nucleic acid, e.g., mRNA is present in PBMCS, e.g., by PCR (such as reverse transcriptase or RT-PCR); and/or detecting whether a cellular-mediated immune response to CMV peptides or proteins is present, e.g., whether PBMCs recognize and/or respond to CMV peptides or proteins, e.g., by administering a CMV skin test by administering CMV proteins or peptides intradermally or subcutaneously or intramuscularly and ascertaining the result of the skin test and/or presenting CMV proteins or peptides to a patient's PBMCs and measuring either the proliferative response of the cells (PMBCs) or the cytokine profile; and/or HLA phenotyping and/or HLA genotyping; and optionally screening a sample from a patient (e.g., sera, blood, SMCs, lesions, etc.) for p53; with initial screening for antibodies to CMV or proteins from CMV, which may optionally be omitted.

The diagnostic method of the invention can also be used to test for stratification of atherosclerosis and/or restenosis risk factors.

The present invention includes demonstrating a relation between the presence of antibodies to CMV at the time of angioplasty, indicating prior exposure to CMV, and the subsequent development of restenosis.

The present invention also provides compositions and methods arising as a consequence of demonstrating that there is such a relation.

The present invention includes a showing of a connection between CMV and restenosis and/or atherosclerosis, especially mechanisms involving the virus, including such as the virus, by inhibiting either the capacity of p53 to block cell cycle progression, or its capacity to initiate apoptosis, enhances SMC accumulation and thereby facilitates development of restenotic lesions.

The present invention additionally provides compositions and methods arising as a consequence of demonstrating that there is such a connection and/or mechanisms.

The invention further comprehends methods for preparing the compositions of the invention.

These and other embodiments are disclosed or are obvious from and encompassed by, the following Detailed Description.

BRIEF DESCRIPTION OF FIGURES

The following Detailed Description, given by way of example, but not intended to limit the invention to specific embodiments described, may be understood in conjunction with the accompanying Figures, incorporated herein by reference, in which:

FIG. 1 shows the influence of prior HCMV infection on cumulative distribution of percent stenosis of target vessels determined by angiography 6 months following DCA (Eighty-five target vessels from 75 patients were divided into two groups based on anti-CMV IgG antibody seropositivity status at study entry. A positive CMV IgG antibody status was defined, prospectively, as a cytomegalisa value of ≧0.25. Vessels from seropositive patients had higher percent stenoses compared with those from seronegative patients (p=0.01));

FIG. 1A shows the incidence of restenosis (>50% diameter narrowing) in the seropositive/seronegative patients;

FIG. 2 shows the cumulative percent distribution of MLD at base line, immediately after the DCA procedure, and at six-month follow-up (See text and Table 2 for detailed statistical analysis);

FIG. 3 shows the cumulative percent distribution of luminal diameter loss index (The loss index (late loss divided by acute gain) was higher in the seropositive than in the seronegative patients (p=0.0005));

FIG. 4 shows the patients' anti-CMV IgG antibody titer status at study entry and six months following the DCA procedure;

FIG. 5 shows patterns of anti-CMV IgG antibodies and T lymphocyte proliferation to CMV antigens in healthy individuals (Serum IgG antibodies for CMV were determined using an ELISA kit (CYTOMEGELISA II, Biowhittaker, Walkersville, Md.). Antibody titers were calculated from standard curves provided by the manufacturer. The threshold value for a “positive” result was that provided by the company, which we used prospectively: an ELISA value of less than 0.25 units was considered a negative result, and a value of 0.25 unit or higher was considered a positive result, indicating prior exposure to CMV. Samples for anti-CMV IgG antibodies were tested in triplicate and in two separate experiments. T lymphocyte proliferative responses were performed in 96-well flat-bottom plates (Costar, Cambridge, Mass.). 100 μl of PBMCs (3×10⁶/ml) was added to each well. PBMCs were cultured at 37° C. with 5% CO₂ in RPMI 1640 (Gibco) containing 5% human AB serum, 2 mM L-glutamine, 100 U/ml penicillin, 100 μg/ml streptomycin and Herpes buffer, with or without exposure to CMV antigens. After 6 days of culture (3 days for PHA stimulation), each well was pulsed with 1 μCi of [³H]thymidine, and harvested 18 hours later. Thymidine incorporation was determined using a model LS1801 β-spectrometer (Beckman Instruments, Fullerton, Calif.). All samples were assayed in triplicate and expressed as the mean counts per minute (cpm). The data are presented as stimulation index (cpm of cultures in the presence of CMV antigens divided by cpm of cultures in the absence of CMV antigens). If a sample had a response to two of the three CMV antigen preparations (heat inactivated supernatants of CMV-infected fibroblasts, CMV-infected cell lysates, or fixed CMV-infected fibroblasts) and the stimulation index in each was above 4.0, the response was considered positive);

FIGS. 6A to D show the percentage of individuals with HLA-B44, DR7 and B35 in different CMV-induced immune response subgroups (HLA typing was performed on PBMCs by the NIH HLA laboratory. The standard NIH microcytotoxicity method was used for HLA class I and some class II typing (K. A. Hopkins, A. van Leeuwen, G. N. Tardiff, W. M. LeFor, in ASHI laboratory manual; Lymophotoxicity testing, Zachary A. A. and G. A. Teresi, Eds., (Lenexa, Kans.: American Society for Histocompatibility and immunogenetics, 1990), pp. 195). Most class II types were determined by PCR (F. M. Marincola et al., J. Immunother. 18, 242 (1995)). Data were analyzed by the chi-square test or Fisher's exact test using the Instat program (GraphPAD Software, San Diego, Calif.). All tests were two-tailed. P values less than 0.05 were considered significant);

FIG. 7 shows HLA-B35 and positive T-cell proliferative response to CMV antigens in CMV-seronegative individuals (The percentage of seronegative individuals with HLA-B35 who developed a T-cell proliferative response to CMV antigens was significantly higher (P=0.02) than the percentage of seronegative individuals without HLA-B35);

FIG. 8 shows the DNA sequence of HCMVgB (Towne strain) (SEQ ID NO:1);

FIGS. 9A and B show the DNA sequence of the H6 promoted HCMVgB and NYVAC sequences flanking the TK locus (SEQ ID NO:2) (the 5′ end of the H6 promoted CMVgB is at position 3447; the CKVgB coding sequence is from position 3324 through position 606);

FIGS. 10A to C show the DNA sequence of a 7351 base pair fragment of canarypox DNA containing the C3 ORF (SEQ ID NO:3) (the C3 ORF is initiated at position 1458 and terminates at position 2897);

FIGS. 11A to C show the DNA sequence of the H6 promoted HCMVgB and ALVAC sequences flanking the C3 locus (SEQ ID NO:4) (the 5′ end of the H6 promoted CMVgB is at position 4425; the CMVgB coding sequence is from position 4301 through position 1581);

FIGS. 12A and B show the DNA sequence of the H6 promoted HCMVgB and NYVAC sequences flanking the ATI locus (SEQ ID NO:5) (the 5′ end of the H6 promoted CMVgB is at position 3348; the CMVgB coding sequence is from position 3224 through position 504);

FIG. 13 shows the DNA sequence of HCMVgB (Towne strain) deleted of its transmembrane region (SEQ ID NO:6);

FIGS. 14A and B show the DNA sequence of the H6 promoted HCMVgB lacking its transmembrane region and NYVAC sequences flanking the ATI locus (SEQ ID NO:7) (the 5′ end of the H6 promoted CMVgB is at position 3173; the CMVgB coding sequence is from position 3050 through position 504);

FIG. 15 shows the DNA sequence of HCMVgB (Towne strain) deleted of its transmembrane region and containing an altered cleavage site (SEQ ID NO:8);

FIGS. 16A and B show the DNA sequence of the H6 promoted HCMVgB lacking its transmembrane region and containing an altered cleavage site plus NYVAC sequences flanking the ATI locus (SEQ ID NO:9) (the 5′ end of the H6 promoted CMVgB is at position 3173; the CMVgB coding sequence is from position 3050 through position 504);

FIG. 17 shows the DNA sequence of HCMVgH (Towne strain) (SEQ ID NO:10);

FIGS. 18A and B show the DNA sequence of the 42K promoted HCMVgH plus NYVAC sequences flanking the I4L locus (SEQ ID NO:11) (the 5′ end of the 42K promoted CMVgH is at position 641; the CMVgH coding sequence is from position 708 through position 2933);

FIGS. 19A and B show the DNA sequence of the 42K promoted CMVgH and ALVAC sequences flanking the C5 locus (SEQ ID NO:13) (the 5′ end of the 42K promoted CMVgH is at position 1664; the CMVgH coding sequence is from position 1730 through position 3955);

FIG. 20 shows the DNA sequence of the 42K promoted CMVgH and WR flanking sequences (SEQ ID NO:13) (the 5′ end of the 42K promoted CMVgH is at position 2457; the CMVgH coding sequence is from position 2391 through 166);

FIG. 21 shows the DNA sequence of HCMV IE1 (AD169 strain) (SEQ ID NO:14);

FIG. 22 shows the DNA sequence of the H6 promoted CMVIE1 and WR flanking sequences (SEQ ID NO:15) (the 5′ end of the H6 promoted CMVIE1 is at position 1796; the CMVIE1 coding sequence is from position 1673 through 201);

FIGS. 23A and B show the DNA sequence of the H6 promoted CMVIE1 and NYVAC sequences flanking the ATI locus (SEQ ID NO:16) (the 5′ end of the H6 promoted CMVIE1 is at position 2030; the CMVIE1 coding sequence is from position 1906 through position 434);

FIG. 24 shows the DNA sequence of HCMVIE1 (AD169 strain) lacking amino acids 292-319 (SEQ ID NO:17);

FIGS. 25A and B show the DNA sequence of the H6 promoted CMVIE1 lacking amino acids 292-319 and NYVAC sequences flanking the ATI locus (SEQ ID NO:18) (the 5′ end of the H6 promoted CHVIE1 is at position 1940; the CMVIE1 coding sequence is from position 1816 through position 434);

FIG. 26 shows the DNA sequence of the Exon 4 segment of HCMVIE1 (AD169 strain) (SEQ ID NO:19);

FIG. 27 shows the DNA sequence of the H6 promoted CMVIE1 Exon 4 segment and NYVAC sequences flanking the I4L locus (SEQ ID NO:20) (the 5′ end of the H6 promoted IE1 Exon 4 is at position 630; the CMVIE1 Exon 4 coding sequence is from position 754 through position 1971);

FIGS. 28A and B show the DNA sequence of the H6 promoted CMVIE1 Exon 4 segment and ALVAC sequences flanking the C5 locus (SEQ ID NO:21) (the 5′ end of the H6 promoted IE1 Exon 4 is at position 1647; the CMVIE1 Exon 4 coding sequence is from position 1771 through position 2988);

FIG. 29 shows the DNA sequence of HCMVIE1 (AD169 strain) lacking amino acids 2-32 (SEQ ID NO:22);

FIG. 30 shows the DNA sequence of the H6 promoted CMVIE1 lacking amino acids 2-32 and NYVAC sequences flanking the I4L locus (SEQ ID NO:23) (the 5′ end of the H6 promoted IE1 lacking amino acids 2-32 is at position 630; the coding sequence for CMVIE1 lacking amino acids 2-32 is from position 754 through position 2133);

FIGS. 31A and B show the DNA sequence of the H6 promoted CMVIE1 lacking amino acids 2-32 and ALVAC sequences flanking the C5 locus (SEQ ID NO:24) (the 5′ end of the H6 promoted IE1 lacking amino acids 2-32 is at position 1647; the CMVIE1 coding sequence for CMVIE1 lacking amino acids 2-32 is from position 1771 through position 3150);

FIG. 32 shows the DNA sequence of HCMV pp65 (Towne strain) (SEQ ID NO:25);

FIG. 33 shows the DNA sequence of the H6 promoted CMVpp65 and NYVAC sequences flanking the HA locus (SEQ ID NO:26) (the 5′ end of the H6 promoted pp65 is at position 476; the CMVpp65 coding sequence is from position 600 through 2282);

FIGS. 34A and B show the DNA sequence of a 3706 base pair fragment of canarypox DNA containing the C6 ORF (SEQ ID NO:27) (the C6 ORF is initiated at position 377 and terminated at position 2254);

FIGS. 35A and B show the DNA sequence of the H6 promoted CMVpp65 and ALVAC sequences flanking the C6 locus (SEQ ID NO:28) (the 5′ end of the H6 promoted pp65 is at position 496; the CMVpp65 coding sequence is from position 620 through 2302);

FIG. 36 shows the DNA sequence of the H6 promoted CMVpp65 and WR flanking sequences (SEQ ID NO:29) (the 5′ end of the H6 promoted pp65 is at position 168; the CMVpp65 coding sequence is from position 292 through 1974);

FIG. 37 shows the DNA sequence of HCMVpp150 (Towne strain) (SEQ ID NO:30);

FIGS. 38A and B show the DNA sequence of the 42K promoted CMVpp150 and NYVAC sequences flanking the ATI locus (SEQ ID NO:31) (the 5′ end of the 42K promoted pp150 is at position 3645; the CMVpp150 coding sequence is from position 3580 through 443);

FIGS. 39A and B show the DNA sequence of the 42K promoted CMVpp150 and ALVAC sequences flanking the C6 locus (SEQ ID NO:32) (the 5′ end of the 42K promoted pp150 is at position 3714; the CMVpp150 coding sequence is from position 3649 through 512);

FIGS. 40A and B show the DNA sequence of the 42K promoted CMVpp150 gene and WR flanking sequences (SEQ ID NO:33) (the 5′ end of the H6 promoted pp150 is at position 3377; the CMVpp150 coding sequence is from position 3312 through 175);

FIGS. 41A and B show the DNA sequence of the 42K promoted HCMVgH and H6 promoted HCMVIE Exon 4 and NYVAC sequences flanking the I4L locus (SEQ ID NO:34) (the 5′ end of the 42K promoted CMVgH is at position 2935; the CMVgH coding sequence is from position 2869 through 644; the 5′ end of the H6 promoted CMVIE Exon 4 is at position 2946; the CMVIE Exon 4 coding sequence is from position 3070 through position 4287);

FIGS. 42A to C show the DNA sequence of the H6 promoted HCMV pp65 and 42K promoted HCMVpp150 and ALVAC sequences flanking the C6 locus (SEQ ID NO:35) (the 5′ end of the H6 promoted CMVpp65 is at position 496; the CMVpp65 coding sequence is from position 620 through 2302; the 5′ end of the 42K promoted CMVpp150 is at position 5554; the CMVpp150 coding sequence is from position 5489 through position 2352);

FIG. 43 shows the DNA sequence of HCMVgL (Towne strain) (SEQ ID NO:36);

FIGS. 44A and B show the DNA sequence of the H6 promoted HCMVgB and H6 promoted HCMVgL and NYVAC sequences flanking the TK locus (SEQ ID NO:37) (the 5′ end of the H6 promoted CMVgB is at position 3447; the CMVgB coding sequence is from position 3324 through position 606; the 5′ end of the H6 promoted CMVgL is at position 3500; the CMVgL coding sequence is from position 3624 through position 4460);

FIG. 45 shows the results of HCMV IE1 CTL stimulation by ALVAC-IE1 (vCP256) (percent cytotoxicity; white bars=WR, black bars=WRIE1, striped bars=nonautologous);

FIG. 46 shows the results of stimulation of HCMV pp65-CTLs by ALVAC-pp65 (vCP260) (human CTLs stimulated in vitro and assayed for HCMV pp65 CTLs using methodology similar to that used for FIG. 49; percent cytotoxity; white bars=WR, black bars=WR-pp65, striped bars=nonautologous);

FIG. 47 shows the results of stimulation of HCMV IE1 CTLs by ALVAC-IE1 (vCP256) (methodology similar to that used for FIG. 49, except that following 6 days incubation for restimulation, the responder mononuclear cells were incubated with immunomagnetic beads coupled to monoclonal anti-human CD3, CD4 or CD8; percent cytotoxicity; white bars=WR, black bars=WR-IE1, striped bars=HLA mismatch);

FIGS. 48A to D show expression of CMV gB by COPAK recombinants in Vero and HeLa cells (cell and medium fractions from infected cells radiolabeled with [S 35] methionine were immune precipitated with guinea pig anti-CMV gB; Vero medium (A), HeLa medium (B), Vero cell (C), and HeLa cell (D) fractions derived from infections by vP993 COPAK parent (lanes 1), vP1126 expressing the entire gB (lanes 2), vP1128 expressing gB without the transmembrane site (lanes 3), and vP1145 expressing the gB without transmembrane and with altered cleavage sites (lanes 4) are shown; far right lane contains molecular weight markers);

FIGS. 49A and B show vaccinia infection of Vero and HeLa cells detected by expression of vaccinia early protein E3L (cell fractions from infected cells radiolabeled with [35 S] methionine were immune precipitated with rabbit anti-p25 (E3L); Vero (A) and HeLa (B) cell fractions derived from infections by vP993 (lanes 1), vP1126 (lanes 2), vP1128 (lanes 3), and vP1145 (lanes 4) are shown; far right lane contains molecular weight markers);

FIG. 50 shows comparison of CMV gB production by Vero, HeLa and MRC-5 cells (SDS-PAGE and western blot analysis were performed on the medium from MRC-5 cells (lanes 1, 4), Vero cells (lanes 2, 5), or HeLa cells (lanes 3, 6) after infection with vP1145 (lanes 1, 2, 3) or vP993 (lanes 4, 5, 6); CMV gB was detected with monoclonal CH380; molecular weight markers are present in lane M);

FIG. 51 shows immunoprecipitation of CMV gB by a panel of monoclonal antibodies and guinea pig anti-gB (radiolabeled medium fractions from Vero cells infected with vP993 (lanes 1), vP1126 (lanes 2), vP1128 (lanes 3), and vP1145 (lanes 4) were immune precipitated with guinea pig anti-CMV gB or with monoclonals 13-127, 13-128, CH380, HCMV 34, or HCMV 37; far left lane contains molecular weight markers);

FIG. 52 shows western blot analysis of fractions and bed material from CMV gB immunoaffinity chromatography columns (column 19 fractions representing eluted gB (lane 5), flow through material (lane 6), and crude gB material applied to the column (lane 7) were analyzed by SDS-PAGE and western blot using monoclonal CH380; included in the assay was bed material from column 19 (lane 2) and column 11 (lane 3), as well as gB purified on column 7 (lane 4); molecular weight markers are present in lane 1);

FIG. 53 shows SDS-PAGE analysis of CMV gB eluted from an immunoaffinity chromatography column (fractions 8.16 through 8.22, eluted from column 8, were electrophoretically separated on a 10% gel under reducing conditions, and stained with silver);

FIG. 54 shows SDS-PAGE analysis of five batches of immunoaffinity purified CMV gB (samples of batches 1 through 5 (lanes 1-5) were electrophoretically separated on a 10% gel under reducing conditions and stained with Coomassie Blue; Lane M contains molecular weight markers);

FIGS. 55, 55A shows characterization of immunoaffinity purified CMV gB (batch 5, analyzed by SDS-PAGE, as shown in FIGS. 54A and B, was scanned with a densitometer, and bands were defined (lane 7, labels 1 through 8) with FIG. 55A showing a densitometer tracing through lane 7);

FIGS. 56A and B show immunoblot analysis of immunoaffinity purified CMV gB (purified HIV env (lanes 1), affinity purified CMV gB (lanes 2), crude CMV gB (lane (B3), or monoclonal CH380 (lane A3) were electrophoretically separated on a 10% gel, blotted onto nitrocellulose paper and probed for the presence of mouse IgG H and L chains or CMVgB using goat anti-mouse IgG (A) or monoclonal CH380 (B), respectively; molecular weight markers are present in lanes 4);

FIGS. 57A and B show immunoprecipitation/immunoblot analysis of affinity purified gB (Batch 1 immunoaffinity purified gB(1) or crude gB (B) was immunoprecipitated with monoclonals CH380 (lanes 1), 13-127 (lanes 2), 13-128 (lanes 3), HCMV 37 (lanes 4), or HCMV 34 (lanes 5); the immunoprecipitates were electrophoretically separated on a 10% gel under reducing conditions, blotted onto nitrocellulose and probed for the presence of gB, using guinea pig anti-CMB gB; far left lanes are molecular weight markers);

FIGS. 58A and B show immunoblot analysis of affinity purified CMV gB (Vero cells lysates (lanes A3, B2), CEF lysates (lane A2), vaccinia-infected Vero cells (lane B3), crude CMV gB (lanes 4), affinity purified CMV gB (lanes 5), or purified HIV env (lanes 6) were electrophoretically separated on a 10% gel under reducing conditions, blotted onto nitrocellulose, and probed for the presence of Vero cell proteins using rabbit anti-Vero cells (A), or vaccinia proteins using rabbit anti-vaccinia (B); molecular weight markers are present in lanes 1);

FIGS. 59A-C show the DNA sequence of the H6 promoted HCMVpp65 and 42K promoted HCMVpp150 and ALVAC sequences flanking the C6 locus (SEQ ID NO:38) (The 5′ end of the H6 promoted CMVpp65 is at position 496. The CMVpp65 coding sequence is from position 620 through 2302. The 5′ end of the 42K promoted CMVpp150 is at position 2341. The CMVpp150 coding sequence is from position 2406 through 5543);

FIGS. 60A and B show the DNA sequence of a 5798 bp fragment of canarypox DNA containing the C₇ ORF (tk) (SEQ ID NO:39) (The C₇ ORF is initiated at position 4412 and terminated at position 4951);

FIGS. 61A and B show the DNA sequence of the H6 promoted HCMVgL gene and ALVAC sequences flanking the C₇ locus (The 5′ end of the H6 promoted CMVgL gene is at position 2136. The CMVgL coding sequence is from position 2260 through 3093);

FIGS. 62A and B show the DNA sequence of the H6 promoted HCMVgL gene and H6 promoted HCMV IE1-exon4 gene and ALVAC sequences flanking the C₇ locus (SEQ ID NO:40) (The 5′ end of the H6 promoted CMVgL gene is at position 3476. The CMVgL coding region is from position 3600 through 4433. The 5′ end of the H6 promoted IE1-exon4 is at position 3469. The CMV IE1-exon4 coding region is from position 3345 through 2128);

FIG. 63 shows the DNA sequence of HCMVgH (SEQ ID NO:41)(Towne strain) deleted of its transmembrane region and cytoplasmic tail;

FIGS. 64A and B show the DNA sequence of the H6 promoted HCMVgL gene and 42K promoted truncated HCMVgH gene and NYVAC sequences flanking the ATI locus (SEQ ID NO:42) (The 5′ end of the H6 promoted CMVgL gene is at position 2669. The CMVgL coding region is from position 2793 through 3626. The 5′ end of the 42K promoted truncated CMVgH gene is at position 2650. The truncated CMVgH coding sequence is from position 2584 through 434);

FIG. 65 shows the DNA sequence of a 3209 base pair fragment of canarypox DNA containing the C5 ORF (SEQ ID NO:43) (the C5 ORF initiates at position 1537 and terminates at position 1857);

FIG. 66 shows the nucleotide sequence of the H6/p53 (wildtype) expression cassette and flanking regions from vCP207 (SEQ ID NO:44);

FIG. 67 shows the murine p53 gene (SEQ ID NO:45);

FIG. 68 shows the coding sequence for the human p53 gene (SEQ ID NO:46);

FIG. 69 shows the nucleotide sequence for RCMVIE1 (DNA) (SEQ ID NO:47);

FIG. 70 shows the nucleotide sequence for RCMVIE2 (DNA) (SEQ ID NO:48);

FIGS. 71A and B show the nucleotide sequence for RCNVIE2 (DNA) (SEQ ID NO:49);

FIG. 72 shows the generation of baculovirus and gene expression with the Bac-To-Bac Expression System;

FIG. 73 shows the map and restriction sites for the pFastBac HT expression vector;

FIG. 74 shows multiple cloning site sequences for the pFastBac HT expression vector;

FIG. 75 shows the nucleotide sequence for HCMVIE2 (DNA) (SEQ ID NO:50);

FIGS. 76A and B, respectively, show Western Blot and Coomassie Blue stained gel (FIG. 76A: lane 1=SF9 insect cell lysate, lane 2=baculovirus RCMVIE1 infected SF9 cell lysate, lane 3=RCMVIE1 purified protein preparation, lane 4=baculovirus RCMVIE2 infected SF9 cell lysate, lane 5=RK-13 cells, lane 6=vP1479 infected RK-13 cell lysate, lane 7=prestained molecular weight markers; FIG. 76B: lane 1=RCMVIE1 purified protein preparation, lane 2=prestained molecular weight markers); and

FIG. 77 shows the nucleotide sequence of the wildtype p53 expression cassette and flanking regions within vP1101 (SEQ ID NO:168).

DETAILED DESCRIPTION

As discussed above, the present invention pertains to methods for diagnosis, prophylaxis and treatment of restenosis and/or atherosclerosis, including detecting cellular mediated immune responses and/or HLA phenotyping and/or genotyping, and administering an agent to reduce viral load in a patient in need of such, for instance administering a vaccine or immunological composition against CMV and/or p53. The vaccine or immunological composition can boost the immune response so that the patient's system consequently reduces viral load.

Examples 1 and 2 show the correlation between CMV and vascular disease, and that while there is a correlation between antibodies to CMV and chances of restenosis occurring, diagnostic methods should include detecting cellular mediated immune response and/or HLA phenotyping and/or genotyping, and methods for treatment or prophylaxis can be aimed at decreasing viral load, such as by administering a vaccine or immunological composition against CMV and/or p53.

Example 1, below, may be summarized as follows:

Background: Recent evidence suggests a potential role of cytomegalovirus (CMV) in the development of restenosis: CMV DNA is present in restenosis lesions from atherectomy specimens, and a CMV immediate early gene protein (IE84) binds to and inhibits p53, a gene product that can block cell cycle progression and initiate apoptosis. These p53-mediated effects may contribute to increased SMC accumulation and thereby predispose to restenosis.

Methods: Seventy-five consecutive patients undergoing directional coronary atherectomy (DCA) for symptomatic CAD were prospectively evaluated by measuring anti-CMV IgG antibodies (before DCA) to determine whether prior CMV exposure increases restenosis risk, as determined by a 6-month post-DCA angiogram.

Results: Following the DCA procedure, minimal luminal diameter was greater in CMV seropositive patients (n=49) than in seronegative patients (3.18±0.51 mm vs 2.89±0.45, P=0.01); at six months, however, the large late luminal diameter loss (1.24±0.83 mm vs 0.68±0.69, P=0.003) and loss index (0.68±0.47 vs 0.36±0.33, P<0.001) experienced by seropositive patients resulted in a significantly higher rate of restenosis (43% vs 8%, P=0.002). Both CMV seropositivity (odds ratio=12.9) and CMV titer (odds ratio=8.1) were independently predictive of restenosis (>50% narrowing) in a multivariable logistic regression model. There was no evidence of acute infection, as anti-CMV IgG antibody titers did not increase over time and anti-CMV IgM antibodies were negative in all patients.

Conclusions: Prior infection with CMV is a strong independent risk factor for restenosis.

In more detail, Example 1 provides the first prospective evidence indicating that prior exposure to CMV, as indicated by the presence of CMV IgG antibodies at the time of coronary angioplasty, is a strong independent risk factor for the subsequent development of restenosis (p=0.002; FIG. 1). The importance of prior exposure to CNV infection as a risk factor is further emphasized by the odds ratio of developing restenosis, which was 9-fold greater in patients exposed to CMV than those without such exposure (Table 3). In contrast, no significantly increased risk was seen with any of the other variables tested, findings generally consistent with the results of other studies, e.g., Bach et al., Thromb. Res. 1994; 74:S55-S67; Hermans et al., J. Cardiovas. Pharmaco. 1993; 22(suppl.4):S445-S57; Feuvre et al., Am. J. Cardiol. 1994; 73:840-844; Dzavik et al., Am. J. Cardiol. 1995; 75:936-938; Stein et al., Circulation 1995; 91:979-989; Foley et al., Circulation 1994; 1239-1251.

Analyses believed to provide more complete information than the results of the simple dichotomous analysis described above (restenosis vs no restenosis), led to the same conclusion—that CMV is an important risk factor in the development of restenosis. Thus, when the degree of stenosis is considered as a continuous variable and the effects of CMV are assessed, seropositive patients had a greater degree of lesion stenosis (p=0.01; FIG. 1, Table 2). With MLD considered as a continuous variable (FIG. 2, Table 2), Applicants found that lesion MLD was greater immediately post DCA in the seropositive patients (p=0.01). However, the CMV seropositive patients experienced a markedly greater late loss (p=0.003) and late loss index (p=0.0005), resulting in a tendency for a smaller MLD and a significantly greater incidence of restenosis (p=0.002).

Given that the processes leading to restenosis are complex and undoubtedly multifactorial, it is all the more compelling that one factor—exposure to CMV—conveys such a high risk. Indeed, it is probably this very potency of CMV as a risk factor that accounts for the significant relation Applicants found between anti-CMV antibodies and the incidence of restenosis despite the moderate patient sample-size studied. Also helping the sensitivity and specificity of the study is the fact that the diagnosis of restenosis in this study was based on angiographic analysis rather than on clinical assessment, which is known to be highly inaccurate in predicting anatomic restenosis. Confidence in the results also derives from the fact that this study was prospective in design, that angiographic readers were blinded as to patients' anti-CMV antibody status, and that analysis of anti-CMV antibody levels was performed without knowledge of the angiographic results.

The association between the development of restenosis and CMV was based on anti-CMV IgG antibodies drawn at the time of the angioplasty procedure. Antibody levels did not increase over the ensuing months. This finding, in conjunction with the fact that IgM antibodies were not elevated, suggest that acute CMV infection with systemic viremia did not occur. Although Applicants do not rule out the possibility of acute viremia occurring shortly after angioplasty, with antibody levels returning to baseline by the 6 month repeat studies, Applicants' results are most compatible with the concept that the virus produced either an abortive infection (viral gene expression limited to immediate early gene products), or that viral replication occurred locally in the absence of systemic viremia.

CMV is a complex virus—it has a large genome with over 200 open reading frames. Thus, it undoubtedly possesses many viral proteins that might influence neointimal accumulation. In addition to the effects of IE84, which as noted hereinabove binds to and inactivates p53, infection of SMCs with CMV leads to the expression and secretion of growth factors, Gonczol et al., J. Gen. Virol. 1984; 65:1833-1837; Alcami et al., J. Gen. Virol. 1991; 72:2765-2770, and CMV infection has been shown to activate NFkB, Kowalik et al., Proc. Natl. Acad. Sci. USA 1993; 90:1107-1111, a transcription factor involved in stimulating a broad range of genes, including those involved in inflammatory and immune responses. The virus also increases leukocyte and platelet adhesion to endothelial cells through induction of cellular expression of adhesion molecules, Grundy et al., Immunology. 1993; 78:405-412; O'Brien et al., J. Clin. Invest. 1993; 92:945-951; Span et al., Eur. J. Clin. Invest. 1991; 21:331-338; Etingin et al., Proc. Natl. Acad. Sci. USA 1993; 90:5153-5156; and induces changes that are procoagulant, Van Dam-Mieras et al., Thromb. Haemost. 1992; 68:364-370; Etingin et al., Cell 1990; 61:657-662; Pryzdial et al., Blood 1994; 84:3749-3757. CMV also increases the activity of the scavenger receptor, and IE72, another IE gene product, increases scavenger receptor gene expression, Zhou et al., Circulation 1995; 92:1-162 (Abstr.); increased accumulation of oxidized LDL within lesion SMCs might contribute to an atherogenic-related process like restenosis. Finally, it has recently been shown that IE72 and IE84 inhibit apoptosis, which could increase neointimal accumulation, Zhu et al., J. Virol. 1995; 69:7960-7970.

Totally unexpectedly, Applicants found a strong association between CMV and hypertension. Thus, there may be an important CMV-hypertension link, such that testing for CMV may be indicative of a predisposition to hypertension and vice versa.

It is possible, although Applicants do not necessarily wish to be bound by any one particular theory, that the relation Applicants observed between CMV infection and subsequent development of restenosis is due to a specific relation between the particular angioplasty procedure used in the present investigation—atherectomy—and that very different results may be observed with other techniques such as balloon angioplasty. This possibility appears very remote, as it is generally believed that the final common pathway of the restenosis process is a healing response to vascular injury, a response that probably would be similar (and therefore influenced in a similar way by CMV) whether the injury were induced by balloon angioplasty or by directional atherectomy. Moreover, adjunct balloon dilatation was in fact performed in 87% of patients. Thus, the particular angioplasty procedure is believed to not be a factor.

It is possible that CMV seropositivity, instead of indicating a causal role of CMV per se in restenosis, is just a marker of another process that is actually the mechanistically contributing factor. However, CMV DNA is present in human restenosis, and a CMV gene product inhibits the transcriptional activity of p53 in human coronary artery smooth muscle cells, Speir et al., Science 1994; 265:391-394, and acute CMV infection increases neointimal formation in a rat balloon injury model, Zhou et al., J. Am. Cell. Cardiol. 1995; (suppl) 242a (Abstr.), which when taken together with the results presented herein, strongly suggest that CMV does indeed play a role in restenosis development. (However, the Abstract of Zhou et al., supra, either individually or in a combination with other documents, cannot be said to teach or suggest the present invention because, in addition to the surprising results in the Examples, Zhou et al., supra concerns an acute infection model, whereas human or animal patients are chronically infected).

The results of the present invention demonstrate that CMV seropositivity provides a powerful means of risk-stratifying patients for the development of restenosis. Thus, the determination (from a simple, standard blood test) that a given patient has less than a 10% chance of developing restenosis (CMV seronegative) vs over a 40% chance (CMV seropositive), when considered together with the patient's specific clinical profile, could importantly influence the clinician's decision as to whether that patient might best benefit from bypass surgery or from angioplasty.

However, as shown by Example 2, the CMV seropositive or seronegative status of a patient, while providing particular statistical chances of developing restenosis (Example 1), is not necessarily in and of itself sufficient in providing a diagnosis as to whether there is a predisposition towards or against (prevention of) restenosis and/or atherosclerosis; but rather, detecting a patient's cell mediated immune response to CMV and/or HLA phenotyping and/or genotyping may be more predictive of such a predisposition.

More particularly, because the type of immune response (cellular vs humoral) to infectious agents can determine disease expression or containment, and because cytomegalovirus (CMV) may contribute to restenosis and atherosclerosis, as reported in Example 2, Applicants tested whether there is a spectrum of humoral vs cellular immunodominant responses to CMV infection in healthy individuals. Four patterns were found: both cellular and humoral; humoral only; no detectable response; and, unexpectedly, cellular only. Applicants then determined whether HLA phenotype influenced the type of response: 50% of individuals with a cellular, but not humoral, immunodominant response had an HLA-B35 allele without HLA-B44; conversely, 43% with a humoral, but not cellular, immunodominant response had HLA-B44 without HLA-B35. These values significantly differed from those of control populations. Thus, genetically-determined, HLA-associated, immunodominant patterns of response to CMV occur and may influence susceptibility to CMV-induced disease, including vascular disease.

Pathogen-induced activation of the cellular and the humoral arms of the immune system are frequently inversely related. This observation has led to important insights relating to the type of immune response (cellular or humoral) that permits some hosts either to succeed in eliminating potential pathogens, or to develop persistence of pathogen and the establishment of chronic or recurrent disease.

Although the humoral arm of the immune system is important mainly for prevention of infection by extracelluar agents, if pathogens gain entry to intracellular sites, the cell-mediated immune response becomes essential to pathogen elimination or control. There is now evidence indicating that the cell-mediated immune response is an important mechanism for eliminating or controlling infectious pathogens that cause chronic disease in humans and in various animal species. Data compatible with this concept come from studies of infectious diseases such as acquired immune deficiency syndrome (AIDS) (S. Rowland-Jones et al., Nat. Med. 1, 59 (1995); M. Clerici, JAMA. 271, 42 (1994)), chronic hepatitis B (B. Rehermann, D. Lau, J. H. Hoofnagle, F. V. Chisari, J. Clin. Invest. 97, 1655 (1996)), and leishmaniasis (S. C. Mendonca, P. M. De Luca, W. Mayrink, T. G. Restom, Am. J. Trop. Med. Hyg. 53, 195 (1995); M. L. Guler et al., Science 271, 984 (1996); N. Noben-Trauth, P. Kropf, I. Muller, Science 271, 987 (1996)). On the other hand, a chronic cell-mediated immune inflammatory response can also lead to disease exacerbation.

Given, as shown in Example 2, that the same HLA molecule that predisposes to a cellular immunodominant response to CMV is also associated with a cellular immune response targeted to HIV and to the P. falciparium parasite (which seems to convey a protective effect in these diseases), these results herein have much broader implications.

Specific HLA molecules, such as HLA-B35, may have unique attributes that facilitate the development of a cellular immunodominant response, implying a mechanism whereby some individuals are resistant to certain infectious diseases (or to cancer), and some are susceptible to the development of diseases characterized by immunopathology (chronic granulomatous diseases and autoimmune disease).

There may be a correlation between this pattern of immune response and either protection from, or exacerbation of, any disease processes caused by CMV, including vascular disease.

Thus, novel therapeutic strategies, such as disclosed herein arise. For instance, the results reported herein allow for favorably altering disease outcome by directing attempts to change the immunodominant phenotype from one that increases disease susceptibility to one that promotes resistance.

More importantly, Example 2 shows that diagnosis for a predisposition towards restenosis from angioplasty or for a predisposition towards atherosclerosis cannot be predicated on merely whether an individual has antibodies against CMV, i.e., any prior correlations between CMV and vascular disease fail to teach or suggest the methods and compositions for diagnosis and therapy or treatment or prophylaxis of the present invention.

For instance, Example 2 demonstrates that detecting cellular immune responses and/or HLA genotyping and/or phenotyping can provide surprisingly better diagnosis. Detection of a cellular mediated response can be more predictive or predisposition to or against (prevention) of restenosis and/or atherosclerosis, since antibody-negative patients, as herein demonstrated can have T-cell responses.

Further, this Examples 1 and 2 show the importance in therapy or treatment or prophylaxis to boost the immune response to CMV and/or p53. Simply, the latent CMV infection is a low grade viral infection that the body cannot rid itself of because there is not sufficient stimulation of immune responses. Therapy, treatment or prophylaxis with a vaccine or immunological composition against CMV and/or p53 can thus boost the immune response to eliminate low levels of CMV, e.g., to reduce activation, and thus provide therapy, treatment or prophylaxis with respect to restenosis and/or atherosclerosis.

And, with the now disclosed causal role of CMV in the development of restenosis, and the showing that measuring antibodies against CMV is not sufficient for predicting predisposition towards or against restenosis and/or atherosclerosis, the therapeutic approaches to the prevention and/or treatment of restenosis and/or atherosclerosis, as herein disclosed, e.g., immunological or vaccine compositions comprising CMV antigens or portions thereof and/or p53 or portions thereof, or such compositions in conjunction with additional therapies or treatments, and methods employing them, as well as the diagnostic methods including detecting cell mediated immune response and/or HLA phenotyping and/or genotyping, are now provided.

Thus, in a general way, the invention provides a composition comprising a CMV antigen or antigens, or portions thereof and/or p53 or a portion thereof, and methods for making and using the composition in treatment, therapy or prophylaxis of restenosis and/or atherosclerosis. The composition can be a vaccine or immunological composition. The antigen(s) and/or p53 or portions thereof can be from in vitro and/or in vivo expression by a plasmid, a recombinant, or from isolation and/or purification from cells expressing the antigen(s) and/or p53, e.g., cells infected with HCMV and subsequent isolation and/or purification.

Techniques for protein purification of native proteins, in general, are as follows:

Briefly, the cells are disrupted and the protein of interest is released into an aqueous “extract”. There are many methods of cellular disintegration, which vary from relatively gentle to vigorous conditions, and the choice of one method over the other is dependent upon the source material. Animal tissues vary from the very easily broken erythrocytes to tough collagenous material such as found in blood vessels and other smooth-muscle containing tissue. Bacteria vary from fairly fragile organisms that can be broken up by digestive enzymes or osmotic shock to more resilient species with thick cell walls, needing vigorous mechanical treatment for disintegration.

Gentle techniques include cell lysis, enzymatic digestion, chemical solubilization, hand homogenization and mincing (or grinding); moderate techniques of cell disintegration include blade homogenization and grinding with abrasive materials, i.e., sand or alumina; and vigorous techniques include french press, ultrasonication, bead mill or Manton-Gaulin homogenization. Each of the aforementioned techniques are art-recognized, and it is well within the scope of knowledge of the skilled artisan to determine the appropriate method of cell disintegration based upon the starting material, and the teachings herein and in the art.

Following cell disintegration, the extract is prepared by centrifuging off insoluble material. At this stage, one may proceed with the purification method, as an extract containing as much of the protein of interest as possible has been prepared, and, where appropriate, particulate and most nonprotein materials have been removed.

Standard techniques of protein purification may be employed to further purify the protein of interest, including: precipitation by taking advantage of the solubility of the protein of interest at varying salt concentrations, precipitation with organic solvents, polymers and other materials, affinity precipitation and selective denaturation; column chromatography, including high performance liquid chromatography (HPLC), ion-exchange, affinity, immuno affinity or dye-ligand chromatography; immunoprecipitation and the use of gel filtration, electrophoretic methods, ultrafiltration and isoelectric focusing. Each of the above-identified methods are well within the knowledge of the skilled artisan, and no undue experimentation is required to purify the native proteins or epitopes of interest of CMV or p53, using the standard methodologies outlined hereinabove, and in the literature, as well as the teachings in the Examples below.

In regard to isolation and/or purification of CMV antigen(s) and/or p53 from cells expressing the antigen(s) and/or p53, in addition to methods discussed in the Examples, mention is made of U.S. Pat. Nos. 4,689,225 (HCMV gA subunit vaccine), 5,180,813 (early envelope glycoprotein and monoclonals to HCMV glycoproteins), and 4,716,104 (detection of HCMV antigens by antibodies reactive to IE of HCMV). The compositions and methods of these patents may be useful in the practice of the present invention.

Accordingly, the composition can comprise a vector comprising exogenous DNA encoding at least one CMV and/or p53 epitope. The epitope can be: IE1 and/or IE2 or a portion thereof; gB; gB with transmembrane deleted therefrom; gH; gL; pp150; pp65; IE1 with amino acids 2-32 deleted therefrom; IE1 with amino acids 292-319 deleted therefrom; IE1 exon 4 segment; gB and gH; gB and pp65; gB, gH and pp65; gB, gH, pp65 and IE1 exon 4 segment; gB, gH, pp65, pp150, and IE1 exon 4 segment; gB, gH, pp65 and pp150; gB, gH, gL, pp65, pp150 and IE1 exon 4 segment; and gB, gH, gL, pp65 and pp150; or portion of such CMV antigens; and/or p53, wild-type or mutant, or a portion thereof; or, more generally, a CMV antigen or portion thereof and/or p53 or a portion thereof; and, such a portion thereof can be an antigenic portion; for instance, an epitope of interest. The vector preferably induces an immune response, more preferably a protective immune response, when administered to a patient. Mention is made of U.S. Pat. Nos. 5,047,320 and 5,075,213, incorporated herein by reference, which relate to DNA probes for HCMV gp64 and HCMV gp64 as a vaccine, such that if desired, an epitope of interest in a composition of the invention can be gp64 or a portion thereof.

The methods for making a vector or recombinant can be by or analogous to the methods disclosed in U.S. Pat. Nos. 4,603,112, 4,769,330, 5,174,993, 5,505,941, 5,338,683, 5,494,807, 4,722,848, WO 94/16716, U.S. application Ser. No. 08/184,009, filed Jan. 19, 1994, WO 96/39491, U.S. application Ser. No. 08/658,665, filed Jun. 5, 1996, Paoletti, “Applications of pox virus vectors to vaccination: An update,” PNAS USA 93:11349-11353, October 1996, Moss, “Genetically engineered poxviruses for recombinant gene expression, vaccination, and safety,” PNAS USA 93:11341-11348, October 1996, Smith et al., U.S. Pat. No. 4,745,051 (recombinant baculovirus), Richardson, C. D. (Editor), Methods in Molecular Biology 39, “Baculovirus Expression Protocols” (1995 Humana Press Inc.), Smith et al., “Production of Huma Beta Interferon in Insect Cells Infected with a Baculovirus Expression Vector,” Molecular and Cellular Biology, December, 1983, Vol. 3, No. 12, p. 2156-2165; Pennock et al., “Strong and Regulated Expression of Escherichia coli B-Galactosidase in Infect Cells with a Baculovirus vector,” Molecular and Cellular Biology March 1984, Vol. 4, No. 3, p. 399-406; EPA 0 370 573 U.S. application Ser. No. 920,197, filed Oct. 16, 1986, EP Patent publication No. 265785, U.S. Pat. No. 4,769,331 (recombinant herpesvirus), Roizman, “The function of herpes simplex virus genes: A primer for genetic engineering of novel vectors,” PNAS USA 93:11307-11312, October 1996, Andreansky et al., “The application of genetically engineered herpes simplex viruses to the treatment of experimental brain tumors,” PNAS USA 93:11313-11318, October 1996, Robertson et al. “Epstein-Barr virus vectors for gene delivery to B lymphocytes,” PNAS USA 93:11334-11340, October 1996, Frolov et al., “Alphavirus-based expression vectors: Strategies and applications,” PNAS USA 93:11371-11377, October 1996, Kitson et al., J. Virol. 65, 3068-3075, 1991; U.S. Pat. Nos. 5,591,439, 5,552,143 (recombinant adenovirus expressing HCMV gB and IE-exon 4), Grunhaus et al., 1992, “Adenovirus as cloning vectors,” Seminars in Virology (Vol. 3) p. 237-52, 1993, Ballay et al. EMBO Journal, vol. 4, p. 3861-65, Graham, Tibtech 8, 85-87, April, 1990, Prevec et al., J. Gen Virol. 70, 429-434, PCT WO91/11525, Felgner et al. (1994), J. Biol. Chem. 269, 2550-2561, Science, 259:1745-49, 1993 and McClements et al., “Immunization with DNA vaccines encoding glycoprotein D or glycoprotein B, alone or in combination, induces protective immunity in animal models of herpes simplex virus-2 disease,” PNAS USA 93:11414-11420, October 1996, and U.S. Pat. Nos. 5,591,639, 5,589,466, and 5,580,859 relating to DNA expression vectors, inter alia.

Recombinant poxviruses can be constructed in two steps known in the art and analogous to the methods for creating synthetic recombinants of poxviruses such as the vaccinia virus and avipox virus described in U.S. Pat. Nos. 4,769,330, 4,772,848, 4,603,112, 5,110,587, 5,179,993, 5,505,941, and 5,494,807, the disclosures of which, like the disclosures of all documents cited herein, are incorporated herein by reference.

First, the DNA gene sequence to be inserted into the virus, e.g., an open reading frame from a non-pox source, is placed into a plasmid construct such as an E. coli plasmid construct into which DNA homologous to a section of DNA of the poxvirus has been inserted. Separately, the DNA gene sequence to be inserted can be ligated to a promoter. The promoter-gene linkage is positioned in the plasmid construct so that the promoter-gene linkage is flanked on both ends by DNA homologous to a DNA sequence flanking a region of pox DNA; for instance, pox DNA containing a nonessential locus (although an essential locus may also be used). The resulting plasmid construct is then amplified, e.g., by growth within E. coli bacteria (Clewell, 1972) and isolated (Clewell et al., 1969; Maniatis et al., 1982). Alternatively, the DNA gene sequence can, without separate ligation to a promoter, merely be placed within the plasmid construct so that the DNA gene sequence is flanked on both ends by DNA homologous to a DNA sequence flanking a region of pox DNA; for instance, a region downstream from an endogenous promoter such that expression of the gene sequence is under control of the promoter and the promoter and coding portion of the DNA gene sequence are thus adjacent.

Second, the isolated plasmid containing the DNA gene sequence to be inserted is transfected into a cell culture, e.g. chick embryo fibroblasts, along with the poxvirus. Recombination between homologous pox DNA in the plasmid and the viral genome respectively gives a poxvirus modified by the presence, e.g., in a nonessential region of its genome, of foreign DNA sequences. The term “foreign” DNA designates exogenous DNA, particularly DNA from a non-pox source, that codes for gene products not ordinarily produced by the genome into which the exogenous DNA is placed.

However, the foregoing is not meant to limit the vectors or recombinants or means for obtaining vectors or recombinants in the present invention, as any vector or recombinant as well as any means for obtaining a vector or recombinant, e.g. a poxvirus-CMV and/or p53 epitope of interest recombinant, may be used to obtain the present invention.

In some embodiments, a poxvirus vector may be desired.

Paoletti, U.S. Pat. No. 5,338,683, incorporated herein by reference, provides poxvirus-herpesvirus recombinants, including vaccinia and avipox virus-herpesvirus recombinants, such as vaccinia and avipox virus-CMV recombinants, and gene products therefrom, useful in the practice of this invention.

A preferred vaccinia vector can have attenuated virulence, such as the NYVAC vector. Preferred avipox vectors include ALVAC (attenuated canarypox virus) and TROVAC (attenuated fowlpox virus). ALVAC and TROVAC are each unimolar species. ALVAC has been deposited with the ATCC, Accession No. VR-2547, under the terms of the Budapest Treaty. ALVAC is an attenuated canarypox virus-based vector that was a plaque-cloned derivative of the licensed canarypox vaccine, Kanapox (Tartaglia et al., 1992). ALVAC has some general properties which are the same as some general properties of Kanapox.

ALVAC-based recombinant viruses expressing extrinsic immunogens have also been demonstrated efficacious as vaccine vectors (Tartaglia et al., 1993a,b). So too have NYVAC-based recombinant viruses expressing extrinsic immunogens. In Paoletti et al., U.S. Pat. No. 5,494,807, incorporated herein by reference, ALVAC-HCMV and NYVAC-HCMV recombinants, e.g., such recombinants expressing HCMV gB, which elicit neutralizing antibodies, cell mediated immunity, and epitope-specific cytotoxic T-lymphocytes, and gene products therefrom, useful in the practice of this invention, are disclosed.

Paoletti et al., PCT publication WO 96/39491, based on U.S. applications Ser. Nos. 08/471,014, filed Jun. 6, 1995, and 08/658,665, filed Jun. 5, 1995, incorporated herein by reference, provides recombinant poxvirus-cytomegalovirus compositions and uses, including NYVAC and ALVAC recombinants, e.g., wherein the exogenous DNA codes for an HCMV protein selected from the group consisting of: gB; gB with transmembrane deleted therefrom; gH; gL; pp150; pp65; IE1; IE1 with amino acids 2-32 deleted therefrom; IE1 with amino acids 292-319 deleted therefrom; IE1 exon 4 segment; gB and gH; gB and pp65; gB, gH and pp65; gB, gH, pp65 and IE1 exon 4 segment; gB, gH, pp65, pp150, and IE1 exon 4 segment; gB, gH, pp65 and pp150; gB, gH, gL, pp65, pp150 and IE1 exon 4 segment; and gB, gH, gL, pp65 and pp150, and gene products therefrom, useful in the practice of this invention.

Paoletti et al. WO 94/16716 based on U.S. applications Ser. Nos. 007,115, filed Jan. 21, 1993, and 184,009, filed Jan. 19, 1994, incorporated herein by reference, provides recombinant viruses containing DNA encoding a cytokine and/or tumor associated antigen, including p53, wild-type or mutant, e.g., a NYVAC or ALVAC recombinant containing DNA coding for p53, wildtype or mutant, useful in the practice of this invention.

From the aforementioned Paoletti patent publications, and the teachings herein, including documents incorporated by reference into this specification, the skilled artisan can construct any desired poxvirus-HCMV and/or p53 recombinant expressing an epitope of interest, without undue experimentation.

Baculovirus, adenovirus, and DNA expression systems are also preferred for the practice of the invention.

With respect to certain vectors or recombinants, such as those whose DNA is infectious, e.g., adenovirus vectors, herpesvirus vectors, and the like, methods analogous to the above-described in vivo recombination technique for poxviruses may be employed for construction of the vector or recombinant containing desired exogenous DNA; but, such recombinants or vectors, with reference to adenovirus only for exemplification, may also be obtained by cleaving adenovirus DNA to obtain cleaved adenovirus DNA, ligating the exogenous DNA to the cleaved adenovirus DNA to obtain hybrid adenovirus-exogenous DNA, tranfecting a cell with the hybrid adenovirus-exogenous DNA, and optionally then recovering adenovirus modified by the presence of the exogenous DNA.

U.S. Pat. Nos. 5,591,439 and 5,552,143, incorporated herein by reference, provide adenovirus-HCMV gB or IE-exon 4 recombinants and gene products therefrom, useful in the practice of this invention. Furthermore, by employing the techniques of these patents, or of other literature concerning adenovirus recombinants, with exogenous DNA of any of U.S. Pat. Nos. 5,047,320, 5,075,213, Paoletti, U.S. Pat. No. 5,338,683, Paoletti et al., U.S. Pat. No. 5,494,807, Paoletti et al., PCT publication WO 96/39491, based on U.S. applications Ser. Nos. 08/471,014, filed Jun. 6, 1995, and 08/658,665, filed Jun. 5, 1995, Paoletti et al. WO 94/16716 based on U.S. applications Ser. Nos. 007,115, filed Jan. 21, 1993, and 184,009, filed Jan. 19, 1994, or other documents cited and incorporated herein, or literature concerning HCMV antigens, epitopes of interest, p53, p53 epitopes of interest, and DNA coding therefor, and the teachings herein, adenovirus embodiments expressing any desired HCMV and/or p53 epitope of interest and obtaining gene products therefrom, are within the ambit of the skilled artisan, without undue experimentation, for practice of this invention.

By employing the techniques of Smith et al., U.S. Pat. No. 4,745,051, incorporated herein by reference, or of other literature concerning baculovirus recombinants, with exogenous DNA of any of U.S. Pat. Nos. 5,047,320, 5,075,213, Paoletti, U.S. Pat. No. 5,338,683, Paoletti et al., U.S. Pat. No. 5,494,807, Paoletti et al., PCT publication WO 96/39491, based on U.S. applications Ser. Nos. 08/471,014, filed Jun. 6, 1995, and 08/658,665, filed Jun. 5, 1995, Paoletti et al. WO 94/16716 based on U.S. applications Ser. Nos. 007,115, filed Jan. 21, 1993, and 184,009, filed Jan. 19, 1994, or other documents cited and incorporated herein, or literature concerning HCMV antigens, epitopes of interest, p53, p53 epitopes of interest, and DNA coding therefor, and teachings herein, baculovirus embodiments expressing any desired HCMV and/or p53 epitope of interest and obtaining gene products therefrom, are within the ambit of the skilled artisan, without undue experimentation, for practice of this invention.

By employing the techniques of U.S. Pat. Nos. 5,591,639, 5,589,466, 5,580,589, incorporated herein by reference, or of other literature concerning DNA expression vectors with exogenous DNA of any of U.S. Pat. Nos. 5,047,320, 5,075,213, Paoletti, U.S. Pat. No. 5,338,683, Paoletti et al., U.S. Pat. No. 5,494,807, Paoletti et al., PCT publication WO 96/39491, based on U.S. applications Ser. Nos. 08/471,014, filed Jun. 6, 1995, and 08/658,665, filed Jun. 5, 1995, Paoletti et al. WO 94/16716 based on U.S. applications Ser. Nos. 007,115, filed Jan. 21, 1993, and 184,009, filed Jan. 19, 1994, or other documents cited and incorporated herein or literature concerning HCMV antigens, epitopes of interest, p53, p53 epitopes of interest, and DNA coding therefor, and the teachings herein, DNA expression vector embodiments expressing any desired HCMV and/or p53 epitope of interest and obtaining gene products therefrom, are within the ambit of the skilled artisan, without undue experimentation, for practice of this invention.

Similarly, any other desired vector or recombinant expressing any desired HCMV and/or p53 epitope of interest and obtaining gene products therefrom, are within the ambit of the skilled artisan, without undue experimentation, from this disclosure and the knowledge in the art, for practice of this invention.

The expression product generated by vectors or recombinants in this invention can also be isolated from infected or transfected cells and used to inoculate patients in a subunit vaccine configuration (composition, or an antigenic or immunological composition).

Further, DNA encoding a CMV and/or p53 epitope(s) of interest can be administered through immunization using alternate appropriately engineered mammalian expression systems including but not limited to other poxviruses, herpesviruses, adenoviruses, alphavirus-based strategies, and naked or formulated DNA-based immunogens. Techniques for engineering such recombinant subunits are known in the art. With respect to techniques for these immunization vehicles and state-of-the-art knowledge mention is particularly made of: Hormaeche and Kahn, Perkus and Paoletti, Shiver et al. all in Concepts in Vaccine Development, Kaufman, S. H. E., ed., Walter deGruytes, New York, 1996, and vectors described in Viruses in Human Gene Therapy, Vos, J. -M. H., ed, Chapman and Hall, Carolina Academic Press, New York, 1995, and in Recombinant Vectors in Vaccine Development, Brown, F., ed., Karger, New York, 1994.

The invention still further provides an antigenic, immunogenic, immunological or vaccine composition for use in therapy, treatment and/or prophylaxis of restenosis and/or atherosclerosis containing the recombinant virus or expression product thereof, and an acceptable carrier or diluent. An immunological composition containing the vector or recombinant virus (or an expression product thereof) elicits an immunological response—local or systemic. The response can, but need not be, protective. An immunogenic composition containing the vector or recombinant virus (or an expression product thereof) likewise elicits a local or systemic immunological response which can, but need not be, protective. An antigenic composition similarly elicits a local or systemic immunological response which can, but need not be, protective. A vaccine composition elicits a local or systemic protective response. Accordingly, the terms “immunological composition”, “antigenic composition” and “immunogenic composition” include a “vaccine composition” (as the three former terms can be protective compositions). A protective response is understood to be a response, such as a humoral and/or secretory and/or cell-mediated response which confers an immunity, with immunity understood to comprise the ability to resist or overcome infection or to overcome infection more easily as compared to a subject not administered the inventive composition, or to better tolerate infection as compared to a subject not administered the inventive composition, e.g., increased resistance to infection.

As to epitopes of interest, one skilled in the art can determine an epitope or immunodominant region of a peptide or polypeptide and ergo the coding DNA therefor from the knowledge of the amino acid and corresponding DNA sequences of the peptide or polypeptide, as well as from the nature of particular amino acids (e.g., size, charge, etc.) and the codon dictionary, without undue experimentation.

A general method for determining which portions of a protein to use in an immunological composition focuses on the size and sequence of the antigen of interest. “In general, large proteins, because they have more potential determinants are better antigens than small ones. The more foreign an antigen, that is the less similar to self configurations which induce tolerance, the more effective it is in provoking an immune response.” Ivan Roitt, Essential Immunology, 1988.

As to size: the skilled artisan can maximize the size of the protein encoded by the DNA sequence to be inserted into the mammalian vector (keeping in mind the insertion limitations of the vector). To minimize the DNA inserted while maximizing the size of the protein expressed, the DNA sequence can exclude introns (regions of a gene which are transcribed but which are subsequently excised from the primary RNA transcript).

At a minimum, the DNA sequence can code for a peptide at least 8 or 9 amino acids long. This is the minimum length that a peptide needs to be in order to stimulate a CD4+T cell response (which recognizes virus infected cells or cancerous cells). A minimum peptide length of 13 to 25 amino acids is useful to stimulate a CD8+T cell response (which recognizes special antigen presenting cells which have engulfed the pathogen). See Kendrew, The Encyclopedia of Molecular Biology (Blackwell Science Ltd 1995). However, as these are minimum lengths, these peptides are likely to generate an immunological response, i.e., an antibody or T cell response; but, for a protective response (as from a vaccine composition), a longer peptide is preferred.

With respect to the sequence, the DNA sequence preferably encodes at least regions of the peptide that generate an antibody response or a T cell response. One method to determine T and B cell epitopes involves epitope mapping. The protein of interest “is fragmented into overlapping peptides with proteolytic enzymes. The individual peptides are then tested for their ability to bind to an antibody elicited by the native protein or to induce T cell or B cell activation. This approach has been particularly useful in mapping T-cell epitopes since the T cell recognizes short linear peptides completed with MHC molecules. The method is less effective for determining B-cell epitopes” since B cell epitopes are often not linear amino acid sequence but rather result from the tertiary structure of the folded three dimensional protein. Janis Kuby, Immunology, pp. 79-80 (1992).

Another method for determining an epitope of interest is to choose the regions of the protein that are hydrophilic. Hydrophilic residues are often on the surface of the protein and are therefore often the regions of the protein which are accessible to the antibody. Janis Kuby, Immunology, p. 81 (1992).

Yet another method for determining an epitope of interest is to perform an X-ray crystallographic analysis of the antigen (full length)-antibody complex. Janis Kuby, Immunology, p. 80 (1992).

Still another method for choosing an epitope of interest which can generate a T cell response is to identify from the protein sequence potential HLA anchor binding motifs which are peptide sequences which are known to be likely to bind to the MHC molecule.

The peptide which is a putative epitope of interest, to generate a T cell response, should be presented in a MHC complex. The peptide preferably contains appropriate anchor motifs for binding to the MHC molecules, and should bind with high enough affinity to generate an immune response. Factors which can be considered are: the HLA type of the patient expected to be immunized, the sequence of the protein, the presence of appropriate anchor motifs and the occurrence of the peptide sequence in other vital cells.

An immune response is generated, in general, as follows: T cells recognize proteins only when the protein has been cleaved into smaller peptides and is presented in a complex called the “major histocompatibility complex MHC” located on another cell's surface. There are two classes of MHC complexes—class I and class II, and each class is made up of many different alleles. Different patients have different types of MHC complex alleles; they are said to have a “different HLA type”.

Class I MHC complexes are found on virtually every cell and present peptides from proteins produced inside the cell. Thus, Class I MHC complexes are useful for killing cells which when infected by viruses or which have become cancerous and as the result of expression of an oncogene. T cells which have a protein called CD4 on their surface, bind to the MHC class I cells and secrete lymphokines. The lymphokines stimulate a response; cells arrive and kill the viral infected cell.

Class II MHC complexes are found only on antigen-presenting cells and are used to present peptides from circulating pathogens which have been endocytosed by the antigen-presenting cells. T cells which have a protein called CD8 bind to the MHC class I cells and kill the cell by exocytosis of lytic granules.

Some guidelines in determining whether a protein contains epitopes of interest which will stimulate a T cell response, include: Peptide length—the peptide should be at least 8 or 9 amino acids long to fit into the MHC class I complex and at least 13-25 amino acids long to fit into a class II MCH complex. This length is a minimum for the peptide to bind to the MHC complex. It is preferred for the peptides to be longer than these lengths because cells may cut the expressed peptides. The peptide should contain an appropriate anchor motif which will enable it to bind to the various class I or class II molecules with high enough specificity to generate an immune response (See Bocchia, M. et al., Specific Binding of Leukemia Oncogene Fusion Protein Peptides to HLA Class I Molecules, Blood 85:2680-2684; Englehard, V H, Structure of peptides associated with class I and class II MHC molecules Ann. Rev. Immunol. 12:181 (1994)). This can be done, without undue experimentation, by comparing the sequence of the protein of interest with published structures of peptides associated with the MHC molecules. Protein epitopes recognized by T cell receptors are peptides generated by enzymatic degradation of the protein molecule and are presented on the cell surface in association with class I or class II MHC molecules.

Further, the skilled artisan can ascertain an epitope of interest by comparing the protein sequence with sequences listed in the protein data base. Regions of the protein which share little or no homology are better choices for being an epitope of that protein and are therefore useful in a vaccine or immunological composition. Regions which share great homology with widely found sequences present in vital cells should be avoided.

Even further, another method is simply to generate or express portions of a protein of interest, generate monoclonal antibodies to those portions of the protein of interest, and then ascertain whether those antibodies inhibit growth in vitro of the pathogen from which the the protein was derived. The skilled artisan can use the other guidelines set forth in this disclosure and in the art for generating or expressing portions of a protein of interest for analysis as to whether antibodies thereto inhibit growth in vitro.

For example, the skilled artisan can generate portions of a protein of interest by: selecting 8 to 9 or 13 to 25 amino acid length portions of the protein, selecting hydrophilic regions, selecting portions shown to bind from X-ray data of the antigen (full length)-antibody complex, selecting regions which differ in sequence from other proteins, selecting potential HLA anchor binding motifs, or any combination of these methods or other methods known in the art.

Epitopes recognized by antibodies are expressed on the surface of a protein. To determine the regions of a protein most likely to stimulate an antibody response one skilled in the art can preferably perform an epitope map, using the general methods described above, or other mapping methods known in the art.

As can be seen from the foregoing, without undue experimentation, from this disclosure and the knowledge in the art, the skilled artisan can ascertain the amino acid and corresponding DNA sequence of a CMV and/or p53 epitope of interest for obtaining a T cell, B cell and/or antibody response. In addition, reference is made to Gefter et al., U.S. Pat. No. 5,019,384, issued May 28, 1991, and the documents it cites, incorporated herein by reference (Note especially the “Relevant Literature” section of this patent, and column 13 of this patent which discloses that: “A large number of epitopes have been defined for a wide variety of organisms of interest. Of particular interest are those epitopes to which neutralizing antibodies are directed. Disclosures of such epitopes are in many of the references cited in the Relevant Literature section.”)

The administration procedure for the vector or recombinant or expression product thereof in the invention, and of compositions of the invention such as immunological, antigenic or vaccine compositions which are prophylactic and/or therapeutic compositions with respect to vascular disease, e.g., atherosclerosis and/or restenosis, can be via a parenteral route (intradermal, intramuscular or subcutaneous). Such an administration enables a systemic immune response. The administration can be via a mucosal route, e.g., oral, nasal, genital, etc. Such an administration enables a local immune response. Direct administration to blood vessels and SMCs (see, e.g., Epstein et al., JACC Vol. 23, No. 6, 1994:1278-88 (and documents cited therein, incorporated herein by reference); Chang et al., Science 267:518-22 (Jan. 27, 1995) (and documents cited therein, incorporated herein by reference)) and; French Patent Application 2723697) are also encompassed within the invention.

Epstein et al., JACC, 23(6): 1278-88 (1994) and Didier et al. (Rhone Poulenc Rorer SA), French Patent Application, publication no. 2,723,697 (Feb. 23, 1996) relate to treatments for restenosis, and Chang et al., Science 267:518-522 (Jan. 27, 1995) is directed to therapy for retinoblastoma.

More generally, the antigenic, immunological or vaccine compositions or therapeutic compositions which are prophylactic and/or therapeutic compositions with respect to vascular disease, e.g., atherosclerosis and/or restenosis (compositions containing the vectors or recombinants of the invention or expression products) can be prepared in accordance with standard techniques well known to those skilled in the pharmaceutical or veterinary arts. Such compositions can be administered in dosages and by techniques well known to those skilled in the medical arts taking into consideration such factors as the age, sex, weight, and condition of the particular patient (e.g., factors such as identified in Example 1), and the route of administration. The compositions can be administered alone, or can be co-administered or sequentially administered with other compositions of the invention or with other prophylactic or therapeutic compositions for decreasing viral load or for targeting SMC proliferation.

Such other compositions can include purified native antigens or epitopes or antigens or epitopes from the expression by a poxvirus recombinant or another vector system (such that compositions can contain more that one epitope of interest from CMV and/or p53); antioxidants which inhibit the cytopathic effect of viral infection, and/or compositions which reduce the transcriptional activity of CMV (transcriptional activity reducer) and/or compositions which decrease reactive oxygen species (ROS) generated by the arachidonic cascade and/or the xanthine/xanthine oxidase system (ROS reducer); or another form of molecular based therapy, e.g., expression of cytotoxic molecules to inhibit proliferation of smooth muscle cells and gene therapy, or antisense strategies to inhibit expression of gene products for cell proliferation. Mention is made of WO 96/24604 relating to compositions and methods for treatment of cardiovascular disease involving genes which are differentially expressed.

The antioxidant can be one or more of Vitamin C, Vitamin E, NAC, PDTC, and the like. For information on ROS, ROS reducers, and antioxidants, mention is made of Ian N. Acworth, Bruce Bailey, “The Handbook of Oxidative Metabolism (ESA, Inc.), e.g., pages i, 1-1, Chapter 2 (“Reactive Oxygen Species”), page 2-1 et seg., Chapter 4 (“Mechanisms of Oxygen Damage”), e.g., page 4-1 et seq., Chapter 5 (“Protection Against Oxidants”), page 5-1 et seq., Chapter 7 (“Diseases Associated With Free Radicals”); Davies, “Oxidative stress: the paradox of aerobic life”, Biochem. Soc. Symp. 61, 1-31; Halliwell, “How to characterize an antioxidant: an update”, Biochem. Soc. Symp. 61, 73-101; all incorporated herein by reference (including documents cited therein).

The transcriptional activity reducer can be an antiviral drug such as gancyclovir and/or acyclovir (which interfere with viral replication), and/or an antioxidant, or the like.

The ROS reducer can be aspirin (acetylsalicylic acid) or a derivative thereof, ASA, indomethacin, oxypurinol, and the like.

Compositions which also can be administered in conjunction with the immunological or vaccine composition in the practice of the invention for prevention or treatment of atherosclerosis and/or restenosis, directed to reducing viral load or burden, include, calcium influx blockers and cyclic nucleotide modulators for inhibiting CMV replication, e.g., as disclosed in U.S. Pat. Nos. 4,663,317, 4,800,081, 4,849,412, acyclic pyrrolo[2,3-D pyrimidine analogs, e.g., as disclosed in U.S. Pat. No. 4,927,830, polysubstituted benzimidazoles, e.g., as disclosed in U.S. Pat. No. 5,360,795, heterocyclic thioamides and analogs, e.g., as disclosed in U.S. Pat. No. 5,543,413, or anti-HCMV pharmaceutical compositions, e.g., as disclosed in U.S. Pat. No. 5,316,768. Mention is also made of U.S. Pat. No. 5,547,992, relating to anti-HCMV polycarbonate oligomers.

An interesting embodiment can include administration of an antiviral drug such as gancyclovir and/or acyclovir.

Such other composition(s) is (are) administered taking into account the aforementioned factors. It is believed that the present invention provides for the first time the use of compositions which target HCMV and are directed to lowering HCMV viral load or burden, as a means for prevention and/or treatment of vascular disease, e.g., restenosis and/or atherosclerosis. Thus, the aforementioned “other composition(s)” (other than HCMV and/or p53 epitope of interest or recombinant or DNA so expressing vaccine or immunological compositions), in another embodiment of the invention, may be administered for the prevention or treatment of atherosclerosis and/or restenosis, without necessarily also administering a HCMV and/or p53 epitope of interest vaccine or immunological composition.

Examples of compositions of the invention include liquid preparations for orifice, e.g., oral, nasal, anal, genital (e.g., vaginal), vascular and/or SMC, etc., administration such as suspensions, syrups or elixirs; and, preparations for parenteral, subcutaneous, intradermal, intramuscular, intravenous, intraarterial (e.g., at site of lesion or plaque), intralymphatic, or intraperitoneal administration (e.g., injectable administration) such as sterile suspensions or emulsions. In such compositions the recombinant may be in admixture with a suitable carrier, diluent, or excipient such as sterile water, physiological saline, glucose or the like.

Antigenic, immunological or vaccine compositions, can contain an adjuvant and an amount of the recombinant or expression product or isolated product to elicit the desired response (although embodiments of the invention do not necessarily need to contain an adjuvant; and, in some instances, embodiments of the invention may be without added adjuvant); or, the gene product or product expressed in vivo can be in a form which is exceptionally immunogenic (e.g., a fusion peptide wherein a first portion of the peptide enhances immunogenicity; see, e.g., Huebner et al., WO 96/40718, published Dec. 19, 1996).

In human applications, alum (aluminum phosphate or aluminum hydroxide) is a typical adjuvant. Saponin and its purified component Quil A, Freund's complete adjuvant and other adjuvants are used in research and veterinary applications. Chemically defined preparations such as muramyl dipeptide, monophosphoryl lipid A, phospholipid conjugates such as those described by Goodman-Snitkoff et al., J. Immunol. 147:410-415 (1991) and incorporated by reference herein, encapsulation of the protein within a proteoliposome as described by Miller et al., J. Exp. Med. 176:1739-1744 (1992) and incorporated by reference herein, and encapsulation of the protein in lipid vesicles such as Novasome™ lipid vesicles (Micro Vesicular Systems, Inc., Nashua, N.H.) can also be used.

The compositions of the invention may be packaged in a single dosage form for immunization by parenteral (i.e., intramuscular, intradermal or subcutaneous) administration or orifice administration, e.g., perlingual (i.e., oral), intragastric, mucosal including intraoral, intraanal, intravaginal, intravenous, intralymphatic, intraarterial (e.g., at site of lesion or plaque), intraperitoneal, and the like administration. And again, the effective dosage and route of administration are determined by the nature of the composition, by the nature of the expression product, by expression level if the vector or recombinant is directly used, and by known factors, such as age, sex, weight, condition and nature of patient, as well as LD₅₀ and other screening procedures which are known and do not require undue experimentation.

Dosages of expressed product or isolated product (e.g., isolated from CMV-infected cells) can range from a few to a few hundred micrograms, e.g., 5 to 500 μg. The inventive vector or recombinant can be administered in any suitable amount to achieve expression at these dosage levels. The inventive vector or recombinant can be administered to a patient or infected or transfected into cells in an amount of about at least 10^(3.5) pfu; more preferably about 10⁴ pfu to about 10¹⁰ pfu, e.g., about 10⁵ pfu to about 10⁹ pfu, for instance about 10⁶ pfu to about 10⁸ pfu. And, if more than one gene product is expressed by more than one recombinant, each recombinant can be administered in these amounts; or, each recombinant can be administered such that there is, in combination, a sum of recombinants comprising these amounts. Other suitable carriers or diluents can be water or a buffered saline, with or without a preservative. The expression product or isolated product or vector or recombinant may be lyophilized for resuspension at the time of administration or can be in solution.

In plasmid compositions, the dosage should be a sufficient amount of plasmid to elicit a response analogous to the expressed antigen compositions; or expression analogous to dosages in expressed antigen compositions; or expression analogous to expression obtained in vivo by recombinant compositions. For instance, suitable quantities of plasmid DNA in plasmid compositions can be 1 ug to 100 mg, preferably 0.1 to 10 mg, but lower levels such as 0.1 to 2 mg or preferably 1-10 ug may be employed. Documents cited herein regarding DNA plasmid vectors may be consulted for the skilled artisan to ascertain other suitable dosages for DNA plasmid vector compositions of the invention, without undue experimentation.

The carrier may also be a polymeric delayed release system. Synthetic polymers are particularly useful in the formulation of a composition having controlled release. An early example of this was the polymerization of methyl methacrylate into spheres having diameters less than one micron to form so-called nano particles, reported by Kreuter, J., Microcapsules and NanoDarticles in Medicine and Pharmacology, (M. Donbrow, ed.) CRC Press, p. 125-148.

Microencapsulation has been applied to the injection of microencapsulated pharmaceuticals to give a controlled release. A number of factors contribute to the selection of a particular polymer for microencapsulation. The reproducibility of polymer synthesis and the microencapsulation process, the cost of the microencapsulation materials and process, the toxicological profile, the requirements for variable release kinetics and the physicochemical compatibility of the polymer and the antigens are all factors that must be considered. Examples of useful polymers are polycarbonates, polyesters, polyurethanes, polyorthoesters and polyamides, particularly those that are biodegradable.

A frequent choice of a carrier for pharmaceuticals and more recently for antigens is poly (d,1-lactide-co-glycolide) (PLGA). This is a biodegradable polyester that has a long history of medical use in erodible sutures, bone plates and other temporary prostheses where it has not exhibited any toxicity. A wide variety of pharmaceuticals including peptides and antigens have been formulated into PLGA microcapsules. A body of data has accumulated on the adaption of PLGA for the controlled release of antigen, for example, as reviewed by Eldridge, J. H., et al., Current Tonics in Microbiology and Immunology, 1989, 146:59-66. The entrapment of antigens in PLGA microspheres of 1 to 10 microns in diameter has been shown to have a remarkable adjuvant effect when administered orally. The PLGA microencapsulation process uses a phase separation of a water-in-oil emulsion. The compound of interest is prepared as an aqueous solution and the PLGA is dissolved in a suitable organic solvents such as methylene chloride and ethyl acetate. These two immiscible solutions are co-emulsified by high-speed stirring. A non-solvent for the polymer is then added, causing precipitation of the polymer around the aqueous droplets to form embryonic microcapsules. The microcapsules are collected, and stabilized with one of an assortment of agents (polyvinyl alcohol (PVA), gelatin, alginates, polyvinylpyrrolidone (PVP), methyl cellulose) and the solvent removed by either drying in vacuo or solvent extraction.

Thus, solid, including solid-containing-liquid, liquid, and gel (including “gel caps”) compositions are envisioned.

Furthermore, the vector or recombinant or expression products therefrom or isolated products can be used to stimulate a response in cells in vitro or ex vivo for subsequent reinfusion into a patient. If the patient is seronegative, the reinfusion is to stimulate an immune response, e.g., an immunological or antigenic response such as active immunization. In a seropositive patient, the reinfusion is to stimulate or boost the immune system against the CMV and/or p53, for prevention or treatment of vascular disease such as restenosis and/or atherosclerosis.

For treatment of restenosis, a HCMV and/or p53 vaccine or immunological composition, alone or with other treatment as herein discussed, may be administered as desired by the skilled medical practitioner, from this disclosure and knowledge in the art, e.g., at the first signs or symptoms of restenosis, or as soon thereafter as desired by the skilled medical practitioner, without any undue experimentation required; and, the administration of the vaccine or immunological composition, alone or with other treatment as herein discussed, may be continued as a regimen, e.g., monthly, bimonthly, biannually, annually, or in some other regimen, by the skilled medical practitioner for such time as is necessary to boost the immune response against CMV and keep it boosted so as to prevent further clogging of blood vessels or further symptoms or signs of restenosis, without any undue experimentation required.

For prevention of restenosis, a HCMV and/or p53 vaccine or immunological composition, alone or with other treatment as herein discussed, may be administered at the first indication of the patient being prone to restenosis, or as soon thereafter as desired by the skilled medical practitioner, e.g., within six months prior to, immediately prior to, or at angioplasty, such as within six weeks prior to, immediately prior to, or at angioplasty, in any desired regimen such as a single administration or multiple administrations in a regimen as desired, e.g., monthly, bi-monthly, biannually, or any combination thereof, without any undue experimentation required. Further, for prevention of restenosis, a HCMV and/or p53 vaccine composition, alone or with other treatment as herein discussed, may be administered after angioplasty in a regimen of single or multiple administrations as desired by the skilled medical practitioner, such as immediately after, within six weeks after, within six months after, and/or within a year after, e.g., monthly, bi-monthly, biannually, annually, or in some other regimen, by the skilled medical practitioner for such time as is necessary to boost the immune response against CMV and keep it boosted so as to prevent clogging of blood vessels or symptoms or signs of restenosis, without any undue experimentation required.

For treatment of atherosclerosis, a HCMV and/or p53 vaccine or immunological composition, alone or with other treatment as herein discussed, may be administered at the first signs or symptoms of atherosclerosis, or as soon thereafter as desired by the skilled medical practitioner, without any undue experimentation required; and, the administration of the vaccine or immunological composition, alone or with other treatment as herein discussed, may be continued as a regimen, e.g., monthly, bi-monthly, biannually, annually, or in some other regimen, by the skilled medical practitioner for such time as is necessary to boost the immune response against CMV and keep it boosted so as to prevent further clogging of blood vessels or further symptoms or signs of atherosclerosis, without any undue experimentation required.

For prevention of atherosclerosis, a HCMV and/or p53 vaccine or immunological composition, alone or with other treatment as herein discussed, may be administered at the first indication of the patient being prone to restenosis and/or atherosclerosis, or as soon thereafter as desired by the skilled medical practitioner, in any desired regimen such as a single administration or multiple administrations in a regimen as desired, e.g., monthly, bi-monthly, biannually, or any combination thereof, without any undue experimentation required, e.g., for such time as is necessary to boost the immune response against CMV and keep it boosted so as to prevent clogging of blood vessels or symptoms or signs of atherosclerosis, without any undue experimentation required.

Further, given the prevalence of HCMV in the population as correlated to age, as discussed above (CMV present: in about 10 to 15% of the adolescent population; in about 40 to 50% of the adult, age 35 population; and in more than 60 to 70% of the adult, over age 65 population), a program of administering a HCMV vaccine or immunological composition from childhood, to reduce the prevalence of HCMV in the population, is yet a further method for preventing atherosclerosis and/or restenosis; and, this program can be annual, bi-annual or some other regimen of administration as desired by the skilled medical practitioner, without undue experimentation.

The therapeutic vaccine or immunological composition of the invention can be administered before the angioplasty to induce maximal cellular immune responses at the time of angioplasty, since the restenotic process happens quickly; however, treatment after angioplasty is not excluded.

As discussed above, the present invention also pertains to diagnostic compositions and methods; and, these diagnostic methods and compositions may be used in conjunction with the therapy and/or treatment and/or prophylactic compositions and methods of the invention.

The method for diagnosis to ascertain a susceptibility to atherosclerosis and/or restenosis can comprise immunologically detecting CMV antibodies, preferably against specific viral proteins that are more specific indicators that the virus has been reactivated, such as IE72, IE84, IE55 and the like. The immunologically detecting can be by ELISA and/or immunoblotting. The Examples below discuss testing patients for antibodies against CMV, as well as testing samples for the presence of CMV epitope(s) of interest, antibodies thereto, and DNA coding therefor. Mention is also made of U.S. Pat. Nos. 5,180,813 and 4,716,104, incorporated herein by reference, relating to early envelop glycoprotein and monoclonals to HCMV glycoproteins, and detection of HCMV antigens by antibodies reactive to IE.

The method can include, in addition or alternatively to detecting the neutralizing antibodies, detecting whether CMV mRNA is present in peripheral blood monocytes (PBMCs), e.g., by PCR (such as RT-PCR) and/or detecting whether a cellular-mediated immune response to CMV peptides or proteins is present, e.g., whether PBMCs recognize and/or respond to CMV peptides or proteins.

To detect whether CMV nucleic acids are in a sample, the skilled artisan can employ DNA for primers, as used in the Examples below, or as in the art, e.g., the Paoletti and Paoletti et al. patents and patent publications discussed herein, U.S. Pat. Nos. 5,569,583, 5,173,402, and 4,762,780, incorporated herein by reference, relating to detection of CMV using primers or DNA sequences, U.S. Pat. Nos. 5,047,320 and 5,075,213, incorporated herein by reference, relating to DNA probes for HCMV gp64 (as well as use of HCMV gp64 as a vaccine), and U.S. Pat. Nos. 5,591,439 and 5,552,143, incorporated herein by reference, relating to adenovirus-HCMV gB and IE-exon 4 recombinants.

For instance, DNA as herein disclosed may be contacted with a specimen from a patient, with that DNA employed as a primer in a polymerase chain reaction. From that the skilled artisan can detect the presence or absence of CMV in the sample, and ergo propensity to or against vascular disease such as restenosis and/or atherosclerosis. The sample can be SMCs, sera, blood, or the like, or samples as used in the art.

This aspect of the invention can relate to a skin test whereby the CMV proteins or peptides are administered subcutaneously or intradermally or intramuscularly, which reflects the patient's capacity to mount a cellular-mediated response targeted to the CMV proteins or peptides. A negative or positive skin test shows patients with prior CMV infection and who are thus susceptible or resistant to atherosclerosis and/or restenosis. A negative skin test, for instance, may show either someone who has never seen the virus (Ab−T− of Example 2) or someone who has seen the virus, but did not make a cellular response (Ab+T− of Example 2).

This aspect of the invention can relate more generally to presenting the patient's PBMCs with CMV proteins or peptides and measuring either the proliferative response of the cells or the cytokine profile to determine whether there is a dominant Th1 (e.g., IL-2, IFN-12, IFNγ) or Th2 (IL-4, IL-10) response.

The CMV proteins or peptides can be purified CMV proteins or peptides from lysates of cells previously infected with CMV, or from recombinant expression of the CMV proteins or peptides or epitopes of interest; and, useful in this aspect of the invention is the CMV and p53 epitopes of interest discussed in the following Examples or as in the art, e.g., the Paoletti and Paoletti et al. patents and patent publications discussed herein, U.S. Pat. Nos. 5,047,320 and 5,075,213, incorporated herein by reference, relating to HCMV gp64 as a vaccine, and U.S. Pat. Nos. 5,591,439 and 5,552,143, incorporated herein by reference, relating to adenovirus-HCMV gB and IE-exon 4 recombinants and products therefrom.

This aspect of the invention can also relate to HLA phenotyping and/or HLA genotyping, as such phenotyping and/or genotyping can be used to predict the susceptibility to CMV-induced vascular disease such as restenosis and/or atherosclerosis (see, e.g., Example 2).

This aspect of the invention can further relate to detection of p53. CMV interacts with p53 in smooth muscle cells (SMCs). p53 present in increased amounts binds to MHC Class I antigens in the SMCs and is processed and presented at the cell surface at an increased rate, resulting in stimulation of T cell response, underlying the antibody responses (whereas normal p53 is immunologically silent). Increased or steady state levels of p53 are present in cancers or when viral oncoproteins bind to p53 (as is the case with CMV).

Thus, detection of p53, e.g., at lesions, can be indicative of the presence of CMV proteins, and an indicator of the presence or absence or restenosis and/or atherosclerosis, or of the propensity to develop vascular disease such as restenosis and/or atherosclerosis. p53, or an epitope thereon, can be obtained from cells, or by recombinant methods, e.g., as discussed in the Examples, for use in this aspect of the invention; or, for use in this aspect of the invention, one can use antibodies elicited by such p53, or an epitope thereon, for detection of the presence of p53.

Accordingly, the diagnostic method can comprise screening a sample from a patient (e.g., sera, blood, SMCs, lesions) for antibodies to CMV and/or for the presence of CMV proteins and/or p53. The method can further comprise: screening a sample from a patient for specific viral proteins and/or antibodies thereto that predict whether the virus has been reactivated such as IE72, IE84, IE55 and the like.

These screenings can employ epitopes of interest as in the Examples, or as in the art, e.g., the Paoletti and Paoletti et al. patents and patent publications discussed herein, U.S. Pat. Nos. 5,047,320 and 5,075,213, incorporated herein by reference, relating to HCMV gp64, and U.S. Pat. Nos. 5,591,439 and 5,552,143, incorporated herein by reference, relating to adenovirus-HCMV gB and IE-exon 4 recombinants, in binding assays, or antibodies elicited therefrom; and, binding assays and purification/isolation procedures with respect to epitopes of interest are included in the Examples, or as in the art, e.g., the Paoletti and Paoletti et al. patents and patent publications discussed herein, U.S. Pat. Nos. 5,047,320 and 5,075,213, incorporated herein by reference, relating to HCMV gp64, and U.S. Pat. Nos. 5,591,439 and 5,552,143, incorporated herein by reference, relating to adenovirus-HCMV gB and IE-exon 4 recombinants, and U.S. Pat. Nos. 5,180,813 and 4,716,104 relating to monoclonals to HCNV glycoproteins and detection of HCMV antigens by antibodies reactive to IE.

These screenings can further comprise detecting whether CMV mRNA is present in PBMCs, e.g., by PCR (such as RT-PCR), e.g., employing DNA as disclosed in the Examples herein, or as in the art, e.g., the Paoletti and Paoletti et al. patents and patent publications discussed herein, U.S. Pat. Nos. 5,047,320 and 5,075,213, incorporated herein by reference, relating to HCMV gp64, and U.S. Pat. Nos. 5,591,439 and 5,552,143, incorporated herein by reference, relating to adenovirus-HCMV gB and IE-exon 4 recombinants; and/or detecting whether a cellular-mediated immune response to CMV peptides or proteins is present, e.g., whether PBMCs recognize and/or respond to CMV peptides or proteins, e.g., by administering a CMV skin test by administering CMV proteins or peptides intradermally or subcutaneously or intramuscularly and ascertaining the result of the skin test and/or presenting CMV proteins or peptides to a patient's PBMCs and measuring either the proliferative response of the cells (PMBCS) or the cytokine profile; and/or HLA phenotyping and/or HLA genotyping; and optionally screening a sample from a patient (e.g., sera, blood, lesions, SMCs, etc.) for p53. With respect to RT-PCR (reverse transcriptase-polymerase chain reaction), reference is made to Luehrsen et al., BioTechniques 22(1):168-174 (1996).

The initial screening for antibodies to CMV may optionally be omitted, such that the diagnostic method can comprise: screening a sample from a patient for specific viral proteins that predict whether the virus has been reactivated such as IE72, IE84, IE55 and the like; and/or detecting whether CKV mRNA is present in PBMCs, e.g., by PCR (such as RT-PCR); and/or detecting whether a cellular-mediated immune response to CMV peptides or proteins is present, e.g., whether PBMCs recognize and/or respond to CMV peptides or proteins, e.g., by administering a CMV skin test by administering CMV proteins or peptides intradermally or subcutaneously or intramuscularly and ascertaining the result of the skin test and/or presenting CMV proteins or peptides to a patient's PBMCs and measuring either the proliferative response of the cells (PMBCs) or the cytokine profile; and/or HLA phenotyping and/or HLA genotyping; and optionally screening a sample from a patient (e.g., sera, blood, SMCs, lesions, etc.) for p53.

In general, the diagnostic methods are to ascertain the presence of or propensity towards or against vascular disease such as restenosis and/or atherosclerosis which evaluate whether an individual has been infected by CMV and/or whether a cellular response is present, wherein the cellular mediated response may be predictive of an ability to fight infection, e.g., predictive of a predisposition to or against (prevention of) vascular disease such as restenosis and/or atherosclerosis. Alternatively, it may be predictive of immunopathology, and thereby predict susceptibility to restenosis and/or atherosclerosis. The diagnostic methods can be for stratification of atherosclerosis and/or restenosis risk.

For instance, the methods of the present invention may be useful in the following scenario: someone presents with coronary artery disease and angioplasty is being considered. The patient would be tested for CMV (Abs or cellular response, etc. as herein). If negative, the patient would be at low risk for restenosis (see Examples 1, 2), so angioplasty is indicated without therapy or treatment, e.g., without pre-angioplasty and/or follow-up treatment or therapy, such as aggresive follow-up. If positive, then the patient has a 40-50% risk of restenosis (see Examples 1, 2), and should probably get treatment or therapy, e.g., pre-angioplasty and/or follow-up to angioplasty, by the administration of a composition according to the invention (see description supra, Examples 3 et seq.), or a combination of both in doses such that the skilled artisan would consider such therapy or treatment “aggressive”.

And, the CMV in the various aspects to which the invention pertains can be of human CMV (HCMV), murine CMV (MCMV) or rat CMV (RCMV) origin, with HCMV and RCMV embodiments preferred.

In addition, the therapeutic and prophylactic methods of the present invention can be performed with respect to other infectious agents causing cardiovascular disease. For instance, an antigen or portion thereof, such as an epitope of interest, or a recombinant, e.g., naked DNA, DNA plasmid, virus, etc. expressing such an antigen etc., in vivo and/or in vitro, of another infectious agent linked to cardiovascular disease may be employed instead of or in addition to the CMV antigen or portion thereof in the present invention.

An example of a particular additional infectious agent is Chlamydia pneumoniae, which has been implicated in coronary artery disease; see, e.g., Peeling et al. Emerging Infectious Diseases 2:307-319 (1996); Saikku et al., Chronic Chlamydia pneumoniae Infection as a Risk Factor for Coronary Heart Disease in the Helsinki Heart Study. Ann Intern Med 1992;116:273-8; Thom et al., Association of Prior Infection With Chlamydia pneumoniae and Angiographically Demonstrated Coronary Artery Disease. JAMA 1992;268:68-72; Melnick et al., Past Infection by Chlamydia pneumoniae Strain TWAR and Asymptomatic Carotid Atherosclerosis. Am J Med 1993;95:499-504; Shor et al., Detection of Chlamydia pneumoniae in coronary arterial fatty streaks and atheromatous plaques. S Afr Med J 1992;82:158-61; Kuo et al., Demonstration of Chlamydia pneumoniae in Atherosclerotic Lesions of Coronary Arteries. J Infect Dis 1993;167:841-9; Muhlestein et al., Increased incidence of Chlamydia species within the coronoary arteries of patients with symptomatic atherosclerotic versus other forms of cardiovascular disease. J Am Coll Cardiol 1996;27:1555-61; Godzik et al., In Vitro Susceptibility of Human Vascular Wall Cells to Infection with Chlamydia pneumoniae. J Clin Microbiol 1995;33:2411-4 (but see Weiss et al., Failure to detect Chlamydia pneumoniae in coronary atheromas of patients undergoing atherectomy. J Infect Dis 1996;173:957-62, which is discounted in view of the overwhelming foregoing citations to the contrary). Similarly, the diagnostic methods can be extended to detecting the presence of such other infectious agents. And, these additional therapeutic, prophylactic and diagnostic methods are all within the ambit of the present invention.

A better understanding of the present invention and of its many advantages will be had from the following examples, given by way of illustration.

EXAMPLES Example 1 Relation Between Antibodies to CMV at Angioplasty and Restenosis

With respect to this Example, reference is made to Zhou et al., “Association Between Prior Cytomegalovirus Infection And The Risk Of Restenosis After Coronary Atherctomy,” Aug. 29, 1996, New England Journal of Medicine, 335:624-630, incorporated herein by reference.

CMV infection of immunocompetent adults is common, see Melnick et al. European Heart Journal, supra, and usually asymptomatic, Jordan et al., Ann. Intern, Med. 1973; 79:153-160., Klacsmann, De. Med. J. 1977; 49:499-509. Like other herpesviruses, CMV persists indefinitely in certain host cells. Bruggeman, Vurchows Arch. B. Cell Pathol. 1993; 64:325-333; Banks et al., Clin. Infect. Dis. 1992; 14:933-941. Certain circumstances such as immunosuppression, Jacobson et al. Ann. Intern. Med. 1988; 108:585-94, or iatrogenically following organ transplantation, Schulman et al., Arch. Intern, Med. 1981; 151:1118-24, CMV can be reactivated and cause serious disease, as can other herpesviruses. Viral replication may contribute to the disease process.

CMV may also contribute to disease processes during abortive infections, Southern et al., Engl. J. Med. 1986; 314:359-67, wherein there is viral gene expression limited to immediate early (IE) gene products without viral replication, see Geist et al., Am. J. Respir. Cell. Mol. Biol. 1991; 5:292-296 (CMV IE gene products affecting expression of human cellular genes involved in inflammation and immunologic responses).

Methods

Patients and Study Design

Patients included in this investigation were part of the OARS trial (Optimal Atherectomy Restenosis Study), which was designed to determine the frequency of restenosis following directional coronary atherectomy (DCA). Follow-up angiographic evaluation was obtained approximately 6 months later. Patients derived solely from one of the four multicenter sites (Washington Hospital Center), which recruited 100 of the total 211 OARS patients. Of these 100 patients, 7 were “de-registered” due to an initial procedural complication or protocol violation; an additional 18 patients failed to obtain follow-up angiographic study, leaving a total of 75 patients included in this study.

The patients ranged from 35 to 78 years (mean 58), and there were 58 men and 17 women. Blood samples were collected before and six months after DCA to assay anti-CMV IgG and IgM antibody status. Blood samples were assayed for anti-CMV antibodies without knowledge of the patients' angiographic status.

Clinical Definitions

The following definitions were used: diabetes—if the patient was taking insulin or oral hypoglycemic agents, or had previously taken them and was currently diet controlled; hypertension—if the patient was diagnosed as having hypertension and/or was being treated with antihypertensive medications or diet; hypercholesterolemia—if the patient had a serum cholesterol value of >240 mg/dl at the time of angioplasty or if the patient was on cholesterol lowering treatment.

Directional Atherectomy Procedure

Optimal directional coronary atherectomy involves 1) initial localized plaque resection followed by 2) circumferential plaque resection using larger devices or higher support balloon pressures, and usually concluded with 3) adjunct low-pressure balloon dilatation. Ultrasound guidance is utilized to optimize results. Of the 75 patients, 65 (87%) had adjunct PTCA resulting in a mean 10% additional reduction in final percent diameter stenosis. Two patients (3%) had stents placed after the atherectomy procedure to treat severe lumen-compromising dissections.

Angiographic Analysis

Cineangiograms were forwarded to the core angiographic laboratory blinded to the results of patients' anti-CMV antibody status. Baseline, post DCA procedural, and late follow-up cineangiograms were analyzed using an automated edge detection algorithm (CMS, MEDIS). Minimal lumen diameter (MLD), interpolated reference diameter, and percent diameter stenosis before and after intervention and on follow-up angiography were measured from two projections; the average of these two values is reported. Acute gain was defined as MLD immediately post DCA minus MLD pre DCA; late loss was defined as MLD immediately post DCA minus MLD at six-month follow-up; loss index was defined as late loss divided by acute gain. Restenosis was defined as a dichotomous endpoint of >50% diameter stenosis at follow-up study in a lesion that had been opened to a <50% narrowing immediately after the DCA procedure.

Assays for CKV Antibodies

Anti-CMV IgG assay. Anti-CMV IgG antibodies were tested by using the ELISA kit (Cytomegelisa II test kit) from BioWhittaker (Walkersville, Md.) according to manufacturer's directions. Patient antibody titers (“cytomegelisa value”) were determined from a standard curve. The threshold value for defining a result as seropositive was determined prospectively, as per the manufacturer: a cytomegelisa value <0.25 units is a negative response, while a value of ≧0.25 units indicates prior exposure to CMV.

Anti-CMV IgM test. Anti-CMV IgM antibodies were tested by using the enzyme-linked antibody capture assay kit (CMV CAP-M) from BioWhittaker (Walersville, Md.), according to the manufacturer's directions. As per the manufacturer, an index value of <0.9 was interpreted as negative for CMV IgM antibodies, while a value of >1.1 was interpreted as positive for CMV IgM.

Statistical Analysis

Statistical analyses of frequency counts were performed by the Chi-Square test or the Fisher's Exact test for small sample sizes, and means were compared by the two-sample t-test. All tests were 2-sided. The odds ratio, for comparing the odds of restenosis in those with a given risk factor to those without the risk factor, was chosen as a measure of risk in this prospective study. Modelling of the dichotomous definition of restenosis outcome was performed using the logistic regression model. Factors affecting loss index were identified using linear regression. The covariates considered were CMV status (as a dichotomous variable), CMV titer (as a continuous variable), diabetes, hypercholesterolemia, hypertension, left anterior descending coronary artery location, small reference vessel size (<3 mm in diameter), a history of recent smoking, gender, age, and whether or not the patient had unstable angina as the indication for DCA. All covariates were examined for importance as predictors of restenosis and loss index univariately, as a group in one multivariate model, and in a stepwise multivariable model.

Patient Characteristics

The patients in this study are of similar age and gender, and have similar vessel lesion distribution as the total OARS cohort (Table 1). suggesting that the subgroup is representative of patients undergoing DCA in the larger study.

Forty-nine of the 75 patients (65%) had positive anti-CMV IgG antibody status at study entry, suggesting that they had prior CMV exposure. This prevalence of CMV seropositivity is similar to that reported in several epidemiologic studies conducted in subjects of similar age. Geist et al., Am. J. Respir. Cell. Mol. Biol. 1991; 5:292-296. Of the 18 patients deleted from study because a 6-month angiogram was not obtained, 11 (61%) were CMV seropositive, a percentage virtually identical to that of the 75 patients included in the study. Restenosis developed in 23 of the 75 patients (31%).

Within the CMV seropositive and seronegative groups the relative prevalence of several factors suspected of conveying some increased risk of developing restenosis (see Table 4) did not differ. The one exception was hypertension, which was present in 59% of the seropositive and in 31% of the seronegative patients (p=0.02). Additional analyses showed, however, that hypertension was unrelated to restenosis (p=0.18).

Correlation Between CMV Seropositivity and Development of Restenosis

By comparing patients' anti-CMV IgG antibody status at study entry with six month angiographic outcome, we found that of the 49 patients with prior CMV exposure, 21 (43%) developed restenosis; only 2 of the 26 patients (8%) without prior CMV exposure developed restenosis (p=0.002; FIG. 1A). Analysis of the data using percent stenosis of target vessels at follow-up as a continuous variable indicated that CMV infection predisposes to more severe stenosis (p=0.01; FIG. 1, Table 2).

The luminal dimensions and percent stenosis at baseline, immediately after the DCA procedure, and at follow-up are presented in Table 2. A plot of the cumulative percent of target vessels against MLD at each of the three time points, is shown in FIG. 2. At baseline, the reference vessel diameter and lesion MLD tended to be larger in the CMV seropositive patients, but there was no difference in percent stenosis. Immediately after the procedure, the seropositive group had a slightly larger lesion MLD (p=0.01), but the mean acute gain was similar. However, the seropositive group had a much greater late loss (p=0.003) and, most importantly, an almost 50% greater loss index than the seronegative group (p=0.0005; Table 2 and FIG. 3).

The Influence of CMV Seropositivity and Other Risk Factors on the Development of Restenosis

Univariate analyses (Table 3) identified CMV status as the only statistically significant predictor of restenosis (odds ratio=9.0, p=0.002). An analysis of the association of mean IgG antibody titers on restenosis confirmed the finding (mean titer=0.66±0.30 units for restenosis patients and 0.44±0.35 for no restenosis; p=0.01). There were no other statistically significant predictors of restenosis among the remaining potential risk factors examined. CMV status and CMV titer maintained their relationship with restenosis in the full multivariate logistic regression models (odds ratios, with 95% confidence intervals:=12.9; 2.3, 71.11, p=0.003, and =8.1; 1.5, 43.2, p=0.01, respectively).

The Influence of CMV Seropositivity and Other Risk Factors on Loss Index

Simple linear regression models show that both CMV titer and the dichotomous CMV status (cytomegelisa values ≧0.25 considered positive for CMV, as defined prospectively) are each strong predictors of loss index (p=0.01 and p=0.002, respectively).

The full multiple regression model for loss index shows CMV, when analyzed either as a continuous titer or a dichotomous variable, to be a persistent and independent predictor over and above the effects of all other model covariates (p=0.03 and p=0.01, respectively). Table 4 contains the results for the full model with CMV titer. No other risk factors gained or lost appreciable importance between univariate and multivariate analysis. Also, a stepwise approach to model selection identified CMV titer (and CMV status) as the only significant prognostic variable for loss index. Although the relationship between CMV titer and restenosis was highly significant (p=0.01), CMV titer explained only 7% of the variation in late loss index (r²=0.07). To put this into perspective, taken as a whole, all the risk factors analyzed in this investigation explain only 11.5% if the total variation in loss index.

To determine whether the effect of CMV differed in subgroups defined by the other potential risk variables analyzed in the study, a two-factor interaction of each with CMV was tested and none found significant.

Evidence Against the Presence of Acute Infection and Systemic Viremia

Assays for anti-CMV IgM antibodies, usually present only early after acute infection, were performed. No anti-CMV IgM antibodies were detected in any of the patients. Also, at approximately the six month time-point of the study (the time of follow-up angioplasty), a second assay to determine IgG anti-CMV antibody titers was performed. There was no significant change in titers (FIG. 4). Most importantly, no patient in the original CMV immunopositive group exhibited a significant increase in titer (>2×), and titers fell to within the negative range in only four CMV seropositive patients (of these four patients, all developed restenosis). In addition, none of the original CMV seronegative patients became seropositive.

Immune Status Against Another Virus

To determine whether the correlation between CMV immunopositivity and restenosis was merely a reflection of either a generalized susceptibility to viral infection or a marker of an increased but non-specific immune responsiveness, we determined whether there was a correlation between pre-existing antibodies to Hepatitis A virus and restenosis (seroposivity to Hepatitis A has approximately the same frequency as seropositivity to CMV). Forty-one percent of the total patient group was seropositive for Hepatitis A virus. However, no significant association with restenosis was found; the restenosis rate was 35.7% for Hepatitis A seropositive patients and 37.5% for Hepatitis A seronegative patients.

This Example provides the first prospective evidence indicating that prior exposure to CMV, as indicated by the presence of CMV IgG antibodies, at the time of coronary angioplasty, is a strong independent risk factor for the subsequent development of restenosis (p=0.002; FIG. 1).

TABLE 1 Comparison between total patient cohort of OARS and the OARS subgroup included in the present study. Total OARS Subgroup studied (N = 199) (N = 75) P value Age 58 ± 11 (36-80) 58 ± 10 (35-78) 100♦ Gender 152 (76%) 58 (77%) 0.868† (male) SVD + DVD* 187 (94%) 73 (97%) 0.525⁺ *SVD, DVD = number of patients with single and double vessel disease respectively. ♦By 2-sample T-test (two tailed) †By X²-text ⁺By Fisher's Exact test (two tailed)

TABLE 2 Influence of anti-CMV IgG seropositive/seronegative status on angiographic results of atherectomy CMV + CMV − (N = 58 vessels) (N = 27 vessels) Mean ± SD Mean ± SD mm mm P-value* PRE Reference diameter 3.23 ± 0.42 3.05 ± 0.48 0.07 MLD 1.29 ± 0.44 1.09 ± 0.33 0.045 Stenosis (%) 60 ± 12 64 ± 11 0.21 IMMED-POST Reference diameter 3.37 ± 0.44 3.21 ± 0.47 0.13 MLD 3.18 ± 0.51 2.89 ± 0.45 0.01 Stenosis (%)  5 ± 13 10 ± 10 0.11 FOLLOW-UP Reference diameter 3.27 ± 0.49 3.08 ± 0.40 0.08 MLD 1.93 ± 0.94 2.20 ± 0.6  0.12 Stenosis (%) 42 ± 25 28 ± 18 0.01 GAIN/LOSS Acute gain 1.90 ± 0.56 1.80 ± 0.55 0.44 Late loss 1.24 ± 0.83 0.68 ± 0.69 0.003 Loss index (%) 68 ± 47 36 ± 33 0.0005 *by 2-sample T-test (two sided)

Reference diameter refers to diameter of the normal segment of vessel adjacent to the stenosis.

MLD=minimal luminal diameter of the stenotic lesion

Definition of gain/loss terms as per Example

TABLE 3 Univariate association of restenosis with potential risk factors. Restenosis* No restenosis (n = 23) (n = 52) N (%) N (%) Odds Ratio (95% Cl) P Value⁺ DMV + 21 (91%) 28 (54%) 9.00 (1.91, 42.38) 0.002 Diabetes 4 (17%) 8 (15%) 1.16 (0.31, 4.31) 1.00  LAD lesion 11 (48%) 25 (48) 0.99 (0.37, 2.64) 0.98 Vessel size (<3 mm dia) 8 (35%) 21 (40%) 0.79 (0.28, 2.19) 0.65 Hypertension 14 (61%) 23 (44%) 1.96 (0.72, 5.33) 0.18 Hypercholesterolemia 7 (30%) 21 (40%) 0.65 (0.23, 1.84) 0.41 smoking 5 (22%) 17 (33%) 0.57 (0.18, 1.8) 0.34 Gender (men) 20 (87%) 38 (73%) 2.44 (0.63, 9.09) 0.19 Unstable angina 17 (74%) 40 (77%) 0.85 (0.27, 2.64) 0.78 *Restenosis defined as dichotomous variable (>50% luminal diameter narrowing) ⁺All p-values by x²-text except† by Fisher's Exact Test (two-tailed).

TABLE 4 Association of potential risk factors with loss index (Full multiple linear regression model) Risk factor Slope p value CMV titer* 0.36 0.025 Diabetes −0.03 0.83 LAD lesion 0.09 0.42 Vessel size (<3 mm dia) −0.03 0.78 Hypertension −0.06 0.62 Hypercholesterolemia 0.06 0.58 Unstable angina −0.06 0.64 Smoking −0.03 0.81 Gender (male) −0.13 0.35 Age 0.01 0.30 *When CMV status is defined as a dichotomous value the association when loss index is even stronger (p = 0.007) than when defined as titer, a continuous variable.

Example 2 Immunodominant Cellular and Rumoral Responses to CNV and their Regulation by Specific HLA Alleles

Human cytomegalovirus (CMV) rarely produces clinically recognizable disease in immunocompetent individuals. However, like other herpesviruses, it persists in the infected host for life and, under certain circumstances, can be reactivated to cause clinically important disease. Most known CMV-related diseases occur in immune-compromised patients—such as the CMV-associated diseases experienced by many patients following organ transplantation (R. H. Rubin and R. B. Colvin, in Kidney transplant rejection; Diagnosis and treatment, G. M. Williams, J. F. Burdick, K. Solez Eds. (New York: Dekker, 1986) pp. 283), and the CMV-induced diseases that complicate the course of AIDS patients (R. D. Schrier, W. R. Freeman, C. A. Wiley, J. A. McCutchan, and the HNRC group, J. Clin. Invest. 95, 1741 (1995)). Clinically important CMV-induced disease, however, may not be limited to immune-compromised subjects, as Example 1 provides the first prospective evidence indicating that prior exposure to CMV, as indicated by the presence of CMV IgG antibodies, at the time of coronary angioplasty, is a strong independent risk factor for the subsequent development of restenosis (p=0.002; FIG. 1); with respect to CMV and the development of vascular diseases such as restenosis following coronary angioplasty, and atherosclerosis, see E. Speir et al., Science 256, 391 (1994); Y. F. Zhou et al., N. Engl. J. Med. 335, 624 (1996); J. L. Melinick, B. L. Petrie, G. R. Dreesman, J. Burek, C. H. McCollum, M. E. DeBakey, Lancet 2, 644 (1983); M. T. Grattan, C. E. Moreno-Cabral, V. A. Starnes, P. E. Oyer, E. B. Stinson, N. E. Shumway, JAMA. 261, 3561 (1989); L. Melnick, E. Adam, M. E. DeBakey, JAMA. 263, 2204 (1990).

With CMV related to these diseases, it is of interest that many more individuals exhibit evidence of prior CMV infection than develop vascular disease. Applicants therefore speculated that certain hosts infected with CMV, although immunocompetent, lack an efficient immune-surveillance system targeted to CMV, and, thereby, have an impaired capacity to eliminate the virus or to prevent its reactivation from latency.

To test this prediction, Applicants determined whether, in immunocompetent individuals, there is a spectrum of humoral vs cellular immunodominant responses to CMV infection. In addition, evidence in studies of patients with HIV and patients with malaria indicate there is a relationship between human leucocyte antigen (HLA) phenotypes to both the type of immunodominant response and the susceptibility or resistance to disease (S. Rowland-Jones et al., Nat. Med. 1, 59 (1995); R. D. Schrier, W. R. Freeman, C. A. Wiley, J. A. McCutchan, and the HNRC group, J. Clin. Invest. 95, 1741 (1995); A. S. Hill et al., Phil. Trans. R. Soc. Lond. B. 346, 379 (1994); A. S. Hill et al., Nature 360, 434 (1992)).

Applicants therefore also determined whether, if divergent immune responses to CMV were found in the study population, the type of response is related to HLA phenotypes. Based on data indicating an association between specific HLA phenotypes and 1) cellular immune protection against the development of AIDS in HIV exposed subjects (S. Rowland-Jones et al., Nat. Med. 1, 59 (1995)), 2) susceptibility to CMV-induced retinitis in patients suffering from AIDS (R. D. Schrier, W. R. Freeman, C. A. Wiley, J. A. McCutchan, and the HNRC group, J. Clin. Invest. 95, 1741 (1995)), and 3) susceptibility to CMV-induced disease in renal transplant patients (G. Blancho, R. Josien, D. Douiliard, J. D. Bignon, A. Cesbron, J. P. Soulillou, Transplantation 54, 871 (1992); Y. J. Kraat, M. H. L. Christiaans, F. H. M. Nieman, P. M. van den Berg-Loonen, J. P. van Hooff, C. A. Bruggeman, Lancet 341, 494 (1993).14, 15), Applicants prospectively examined the hypothesis that in immunocompetent individuals with prior CMV exposure the presence of a cellular immune response to CMV would be associated with HLA-B35, whereas its lack would be associated with HLA-DR7 and HLA-B44.

Fifty healthy individuals who volunteered, under an NIH IRB-approved protocol, to donate blood to the Transfusion Medicine Department, National Institute of Health (NIH) were entered into this study. They consisted of 32 (64%) men and 18 (36%) women, and 32 (64%) Caucasians, 17 (34%) Blacks and 1 (2%) Asian. Their ages ranged from 25 to 62 years (mean 40). The HLA frequencies in these study individuals were similar to the reported HLA frequencies in the North American population (T. D. Lee, in The HLA system; Distribution of HLA antigens, J. Lee, Ed. (New York: Springer-Verlag, 1990), pp. 141) (see also below).

To determine whether there are immunodominant humoral and cellular responses to CMV antigens in healthy individuals, all blood samples were tested for 1) anti-CMV IgG antibodies, using an enzyme-linked immunosorbent assay (ELISA), and 2) the ability of T lymphocytes, obtained from peripheral blood mononuclear cells (PBMCs), to proliferate in response to CMV antigens.

In particular, a blood sample from each individual was obtained from the Transfusion Medicine Department, NIH (Bethesda, Md.). PBMCs were separated from whole blood on lymphocyte separation medium (Organon Teknika Corp., Durham, N.C.) by centrifugation at 1,800 rpm for 25 min at room temperature. The separated cells were collected and washed twice in PBS (Gibco, Laboratories, Grand Island, N.Y.). The number of viable cells was determined by trypan blue exclusion and hemacytometer. PBMCs were then cryopreserved in aliquots in liquid nitrogen until used.

CMV antigens were derived from CMV-infected human fibroblasts.

In particular, Human CMV, Towne strain, was obtained from the American Type Culture Collection (ATCC) (Rockville, Md.) and grown in human fibroblasts (HEL299; ATCC) for preparation of the viral antigens. Growth media consisted of Minimum Essential Medium (Gibco) supplemented with 2% fetal bovine serum and antibiotics. Virus titer was measured on HEL299 cells.

The published protocols for CMV antigen preparations were followed, and were as follows:

Briefly, CMV antigens were prepared with 1) heat inactivated CMV (1 hour at 56° C.) that was obtained from supernatants of CMV-infected fibroblasts—final concentration of virus was 10⁵ plaque-forming units (pfu) before inactivation (R. D. Schrier et al., in Y. F. Zhou et al., N. Engl. J. Med. 335, 624 (1996)); 2) cell lysates of CMV-infected fibroblasts by repeated freezing and thawing (G. J. Boland, R. J. Hene, C. Ververs, M. A. M. De Haan, G. C. De Gast, Clin. Exp. Immunol. 94, 306 (1993); and 3) 0.08% glutaraldehyde fixed CMV-infected fibroblast cells (P. J. Converse, A. D. Hess, P. J. Tutschka, G. W. Santos, Infect. Immun. 41, 1226 (1983). Both cell lysates and fixed cells were prepared from 2×10⁶/ml cells by infecting a 90% confluent monolayer of human fibroblasts with CMV at a multiplicity of infection (MOI) of 10. Cells were collected by centrifugation when they showed 50% cytopathic effect. The large stocks were aliquoted and stored at −70° C. Controls for the CMV antigens were obtained from noninfected fibroblasts (mock-infected cells), prepared exactly as described for CMV-infected cells.

Anti-CMV IgG antibodies were detected in 23/50 (46%) of individuals, and CMV-induced T lymphocyte proliferative responses developed in 21/50 (42%). No proliferative response was observed in these individuals when their PBMCs were stimulated with antigens derived from mock-infected fibroblasts, or cultured with medium alone.

Positive controls included: 1) 3 days of stimulation with PHA (Gibco) diluted 1:200; 2) influenza A/Bangkok RX73 (grown in embryonated eggs and used as infectious allantoic fluid at an infectivity of 2×10⁴ tissue culture infectious dose₅₀/well) at a final dilution of 1:1,000; 3) Candida antigen (Greer Laboratories, Inc., Lenoir, N.C.), at a final dilution of 20 mg/ml; 4) a pool of irradiated (5,000 rad) PBMCs from three unrelated healthy donors (2×10⁶/ml). Negative controls were derived from non-infected (mock-infected) fibroblasts and culture medium alone.

The positive proliferative responses to other antigenic stimuli were: 29/50 (58%) to influenza A plus candida antigens, and 35/50 (70%) to allogenic cells. All 50 individuals responded to phytohaemagglutinin (PHA).

FIG. 5 shows the patterns of anti-CMV IgG antibodies and T lymphocyte proliferation to CMV antigens. Of the 50 individuals, nine (18%) had both anti-CMV IgG antibodies and a T-cell proliferative response to CMV antigens (referred to as the antibody positive/T lymphocyte proliferation positive subgroup). Fourteen (28%) who had anti-CMV antibodies did not show a CMV-induced T-lymphocyte response (referred to as the antibody positive/T lymphocyte proliferation negative subgroup). There were 15 individuals (30%) who were negative for both antibodies and T lymphocyte proliferation to CMV (referred to as the antibody negative/T lymphocyte proliferation negative subgroup).

Unexpectedly, 12 (24%) individuals who did not produce anti-CMV IgG antibodies had positive proliferative responses to CMV antigens (referred to as the antibody negative/T lymphocyte proliferation positive subgroup).

These results demonstrate that immunodominant phenotypes directed against CMV are present in immunocompetent individuals. Of interest, 44% of the 27 individuals who were seronegative for CMV antibodies (and therefore, by conventional criteria, would not be considered to have been exposed to CMV) had T lymphocyte proliferative responses to CMV antigens. This particular subgroup, which displayed a dominant cellular immune response to CMV, constituted 24% of the total population.

To determine whether the immune response to CMV infection is related to specific HLA phenotypes, allelic frequencies for HLA class I and class II molecules were analyzed.

The frequency in the North American population (T. D. Lee, in The HLA system; Distribution of HLA antigens, J. Lee, Ed. (New York: Springer-Verlag, 1990), pp. 141) of the specific HLA alleles we prospectively examined is 24% for B44, 26% for DR7, and 18% for B35. There were no significant differences in the HLA allelic frequencies between this control population and the total population, which had allelic frequencies of 30% for B44, 28% for DR7, and 14% for B35. Nor were there significant differences in allelic frequencies between either of these two groups and the antibody negative/T lymphocyte proliferation negative subgroup, which had allelic frequencies of 40% for HLA-B44, 27% for DR7 and 7% for B35 (FIG. 6D). This latter subgroup can probably be considered to consist of individuals who have not been exposed to CMV infection (although some may have had a prior infection following which the virus was either successfully cleared or has remained latent).

In contrast, the remaining subgroups, characterized by their immunodominant response to CMV antigens, demonstrated marked differences in HLA allelic frequency when compared to that of the North American population or the total study population. Thus, neither of the two antibody-positive groups (one characterized by a positive T lymphocyte proliferative response to CMV antigens (FIG. 6A) and the other with a negative proliferative response (FIG. 6B)) contained any individuals carrying the HLA-B35 allele (P<0.05 vs North American and total study populations).

Conversely, in the cellular immunodominant subgroup (CMV-seronegative individuals who were positive for CMV-induced T lymphocyte proliferation; FIG. 6C), none carried HLA-B44, only 8% had DR7, but 50% carried HLA-B35. Both the lower frequency of HLA-B44 (but not DR7) and the higher frequency of HLA-B35 in this cellular immunodominant subgroup are significantly different from the corresponding allelic frequencies in our total study population (P=0.03 for HLA-B44 and P=0.01 for B35) and in antibody negative/proliferation negative individuals (P=0.02 for HLA-B44 and P=0.02 for B35). Although the difference remained highly significant when the allelic frequency for HLA-B35 was compared to that of the North American population, that for HLA-B44 was only of marginal significance (P=0.01 for B35 and P=0.08 for HLA-B44).

To determine whether carrying the HLA-B35 allele uniquely predisposes to a cellular immune response to CMV, the relative frequency of a positive T-cell proliferative response to CMV antigens of those individuals with and those without HLA-B35 was compared. A total of 7 individuals carried HLA-B35, and all were CMV-seronegative. Most importantly, 6 of these 7 (86%) had positive T lymphocyte proliferative responses to CMV antigens (FIG. 7). This is in contrast to 6/20 (30%) of the seronegative individuals without B35 (P=0.02).

Applicants also determined the presence of additional HLA alleles (18 HLA-A alleles, 25 HLA-B, 8 HLA-Cw, 11 HLA-DR, 7 HLA-DRw and 8 HLA-DQ) not prospectively identified as potential determinants of immunodominant response.

Additional HLA phenotypes analyzed were: A1-3, A11, A23, A24, A26, A28-34, A36, A66, A68, A74; B7, B8, B13, B14, B18, B27, B37-42, B51, B53, B55, B57, B58, B60-63, B70-72, B81; Cw1-8; DR1, DR3, DR4, DR9-15, DR18, DRw52, DRw53, DRw3*01-3*03, DRw4*01, DRw5*01 and DQ1-8.

Analysis failed to reveal any significant correlations with cell or antibody immunodominant responses.

Without wishing to necessarily be bound by any one particular theory, Applicants do not rule out that the association between HLA-B35 and a cellular immunodominant response to CMV may be due to a closely-linked but unrelated gene. However, it is of note that HLA-B35, which now has been identified as consisting of a large family of homologous gene products, also is associated with an immunodominant cellular response characterized by the presence of cytotoxic T lymphocytes (CTLs) in subjects exposed to HIV-1 or HIV-2 (S. Rowland-Jones et al., Nat. Med. 1, 59 (1995)), and with the recognition of epitopes of the Plasmodium falciparum malaria parasite, resulting in the generation of specific CTLs (A. S. Hill et al., Phil. Trans. R. Soc. Lond. B. 346, 379 (1994)). The data from these studies further suggested that the cellular immune responses associated with HLA-B35 conveyed protection against the development of AIDS (Rowland et al., supra) and of severe malaria (Hill et al., supra).

Applicants findings demonstrate the association of HLA-B35 with T cell proliferative responses to CMV antigens. This proliferative response has not been shown to be restricted by CD4⁺ and/or CD8⁺ T cells, it is noteworthy that the most common CMV-specific CTLs present in CMV-seropositive healthy blood donors was recently demonstrated to be targeted to pp65, a CMV matrix protein, which was found to contain at least three pp65-specific CTL peptides restricted by HLA-B35. CTLs of seronegative individuals may target the same or different CMV proteins.

It has been pointed out that the high polymorphism and redundancy of the mammalian MHC makes it difficult to identify a particular MHC haplotype determining resistance or susceptibility to an infectious pathogen in humans. Although Applicants have not demonstrated a correlation between HLA phenotype and resistance or susceptibility to CMV-related disease, these results demonstrate that some immune competent individuals are genetically predisposed, in an HLA dependent manner, to respond to CMV with a cellular immune response in the absence of a humoral response. Given that the same HLA molecule that predisposes to a cellular immunodominant response to CMV is also associated with a cellular immune response targeted to HIV and to the P. falciparium parasite (which seems to convey a protective effect in these diseases), these results have much broader implications.

Specific HLA molecules, such as HLA-B35, may have unique attributes that facilitate the development of a cellular immunodominant response, implying a mechanism whereby some individuals are resistant to certain infectious diseases (or to cancer), and some are susceptible to the development of diseases characterized by immunopathology (chronic granulomatous diseases and autoimmune disease).

There may be a correlation between this pattern of immune response and either protection from, or exacerbation of, any disease processes caused by CMV. Thus, novel therapeutic strategies, such as herein arise. For instance, these results allow for favorably altering disease outcome by directing attempts to change the immunodominant phenotype from one that increases disease susceptibility to one that promotes resistance.

More importantly, this Example shows that diagnosis for a predisposition towards restenosis from angioplasty or for a predisposition towards atherosclerosis cannot be predicated on merely whether an individual has antibodies against CMV, i.e., any prior correlations between CMV and vascular disease fail to teach or suggest the methods and compositions for diagnosis and therapy or treatment or prophylaxis of the present invention. For instance, this Example demonstrates that detecting cellular immune responses and/or HLA genotyping and/or phenotyping can provide surprisingly better diagnosis. Detection of a cellular mediated response can be more predictive or predisposition to or against (prevention) of restenosis and/or atherosclerosis, since antibody-negative patients, as herein demonstrated can have T-cell responses.

Further, this Example, with Example 1 shows the importance in therapy or treatment or prophylaxis to boost the immune response to CMV and/or p53. Simply, the latent CMV infection is a low grade viral infection that the body cannot rid itself of because there is not sufficient stimulation of immune responses. Therapy, treatment or prophylaxis with a vaccine or immunological composition against CMV and/or p53 can thus boost the immune response to knock out low levels of CMV from the body, and thus provide therapy, treatment or prophylaxis with respect to restenosis and/or atherosclerosis.

Example 3 Poxvirus-CXV Recombinants

Reference is made to PCT WO 96/39491, incorporated herein by reference, with respect to this Example, especially the Examples thereof from Example 12, and the Figures thereof cited in those Examples such as Figures from FIG. 12, and FIG. 8.

DNA Cloning and Synthesis. Plasmids were constructed, screened and grown by standard procedures (Maniatis et al., 1982; Perkus et al., 1985; Piccini et al., 1987). Restriction endonucleases were obtained from Bethesda Research Laboratories, Gaithersburg, Md., New England Biolabs, Beverly, Mass.; and Boehringer Mannheim Biochemicals, Indianapolis, Ind. Klenow fragment of E. coli polymerase was obtained from Boehringer Mannheim Biochemicals. BAL-31 exonuclease and phage T4 DNA ligase were obtained from New England Biolabs. The reagents were used as specified by the various suppliers.

Synthetic oligodeoxyribonucleotides were prepared on a Biosearch 8750 or Applied Biosystems 380B DNA synthesizer as previously described (Perkus et al., 1989). DNA sequencing was performed by the dideoxy-chain termination method (Sanger et al., 1977) using Sequenase (Tabor et al., 1987) as previously described (Guo et al., 1989). DNA amplification by polymerase chain reaction (PCR) for sequence verification (Engelke et al., 1988) was performed using custom synthesized oligonucleotide primers and GeneAmp DNA amplification Reagent Kit (Perkin Elmer Cetus, Norwalk, Conn.) in an automated Perkin Elmer Cetus DNA Thermal Cycler. Excess DNA sequences were deleted from plasmids by restriction endonuclease digestion followed by limited digestion by BAL-31 exonuclease and mutagenesis (Mandecki, 1986) using synthetic oligonucleotides.

Cells, Virus, and Transfection. The origins and conditions of cultivation of the Copenhagen strain of vaccinia virus has been previously described (Guo et al., 1989). Generation of recombinant virus by recombination, in situ hybridization of nitrocellulose filters and screening for B-galactosidase activity are as previously described (Piccini et al., 1987).

The origins and conditions of cultivation of the Copenhagen strain of vaccinia virus and NYVAC has been previously described (Guo et al., 1989; Tartaglia et al., 1992). Generation of recombinant virus by recombination, in situ hybridization of nitrocellulose filters and screening for B-galactosidase activity are as previously described (Panicali et al., 1982; Perkus et al., 1989).

The parental canarypox virus (Rentschler strain) is a vaccinal strain for canaries. The vaccine strain was obtained from a wild type isolate and attenuated through more than 200 serial passages on chick embryo fibroblasts. A master viral seed was subjected to four successive plaque purifications under agar and one plaque clone was amplified through five additional passages after which the stock virus was used as the parental virus in in vitro recombination tests. The plaque purified canarypox isolate is designated ALVAC.

Example 3.1 Cloning of HCMV gB in Poxvirus Vectors

Cloning of the HCMV gB gene into vaccinia donor plasmid, pMP22BHP. The 4800 bp HindIII-BamHI fragment of the HindIII D fragment of the HCMV DNA (Towne strain) was cloned into the 2800 bp HindIII-BamHI fragment of the plasmid pIBI24 (International Biotechnologies, Inc., New Haven, Conn.). By in vitro mutagenesis (Kunkel, 1985) using the oligonucleotides CMVM5 (SEQ ID NO:51) (5′-GCCTCATCGCTGCTGGATATCCGTTAAGTTTGTATCGTAATGGAATCCAGGATCTG-3′) and CMVM3 (SEQ ID NO:52) (5″-GACAGAGACTTGTGATTTTTATAAGCTTCGTAAGCTGTCA-3′), the gB gene was modified to be expressed under the control of the vaccinia H6 promoter (Taylor et al., 1988a,b; Perkus et al., 1989). The plasmid containing the modified gB was designated 24CMVgB (5+3). The DNA sequence of the CMVgB gene is shown in FIG. 8 (SEQ ID NO:1).

Plasmid pMP2VCL (containing a polylinker region with vaccinia sequences upstream of the K1L host range gene) was digested within the polylinker with HindIII and XhoI and ligated to annealed oligonucleotides SPHPRHA A through D generating SP131 containing a HindIII site, H6 promoter −124 through −1 (Perkus et al., 1989) and a polylinker region.

SPHPRHA A (SEQ ID NO: 53) (5′- AGCTTCTTTATTCTATACTTAAAAAGTGAAAATAAATACAAAGGTTCTTGAGGGT-3′) SPHPRHA B (SEQ ID NO: 54) (5′- TGTGTTAAATTGAAAGCGAGAAATAATCATAAATTATTTCATTATCGCGATATCCGTTAA GTTTGTATCGTAC-3′) SPHPRHA C (SEQ ID NO: 55) (3′- TTATTAGTATTTAATAAAGTAATAGCGCTATAGGCAATTCAAACATAGCATGAGCT-5′) SPHPRHA D (SEQ ID NO: 56) (3′- AGAAATAAGATATGAATTTTTCACTTTTATTTATGTTTCCAAGAACTCCCAACACAATTT AACTTTCGCTCT-5′).

The 2900 bp EcoRV-BamHI fragment of 24CMVgB (5+3) was cloned into the 3100 bp EcoRV-BglII fragment of SP131. This cloning step put the gB gene under the control of the H6 promoter. The resulting plasmid was designated SP131CMVgB.

Plasmid pSD22-H contains a 2.9 kb BglII fragment derived from the HindIII F region of the WR strain of vaccinia virus ligated into the BamHI site of pUC8. The unique BamHI site in pSD22-H is a nonessential site used as an insertion locus for foreign genes (Panicali and Paoletti, 1982). Plasmid pMP22BHP is a derivative of pSD22-H in which the unique BamHI site was modified by the addition of an expanded polylinker region for the insertion of foreign DNA. Plasmid pMP22BHP was digested with HindIII and ligated to a 2.9 kb HindIII fragment from SP131CMVgB (containing the H6 promoted gB gene) generating plasmid SAg22CMVgB. To modify the polylinker region in sAg22CMVgB, the plasmid was digested with BamHI followed by partial digestion with HindIII and purified. Ligation to a 50 bp BamHI/HindIII polylinker derived from IBI24 resulted in plasmid 22CMVgB.

Cloning of the HCMVgB gene into NYVAC donor plasmid pSD542. Plasmid pSD542 (a NYVAC TK locus donor plasmid) was derived from plasmid pSD513 (Tartaglia et al., 1992). The polylinker region in pSD513 was modified by cutting with PstI/BamHI and ligating to annealed synthetic oligonucleotides MPSYN288 (SEQ ID NO:57) (5′-GGTCGACGGATCCT-3′) and MPSYN289 (SEQ ID NO:58) (5′-GATCAGGATCCGTCGACCTGCA-3′) resulting in plasmid pSD542.

22CMVgB was digested with BamHI and NsiI to generate a fragment containing the H6 promoter and part of the gB gene, and with NsiI and PstI to generate a fragment containing the remainder of the gB gene. These two fragments were ligated to pSD542 that had been digested with BamHI and PstI within its' polylinker creating the NYVAC donor plasmid 542CMVgB. The DNA sequence of the CMVgB gene and flanking sequences contained in 542CMVgB is shown in FIGS. 9A and B (SEQ ID NO:2).

Cloning of the HCMV gB gene into the ALVAC donor plasmid CP3LVOH6. An 8.5 kb canarypox BglII fragment was cloned in the BaHI site of pBS-SK plasmid vector (Stratagene, La Jolla, Calif.) to form pWW5. Nucleotide sequence analysis revealed a reading frame designated C3 initiated at position 1458 and terminated at position 2897 in the sequence in FIGS. 10A-C (SEQ ID NO:3). In order to construct a donor plasmid for insertion of foreign genes into the C3 locus with the complete excision of the C3 open reading frame, PCR primers were used to amplify the 5′ and 3′ sequences relative to C3. Primers for the 5′ sequence were RG277 (SEQ ID NO:59) (5′-CAGTTGGTACCACTGGTATTTTATTTCAG-3′) and RG278 (SEQ ID NO:60) (5′-TATCTGAATTCCTGCAGCCCGGGTTTTTATAGCTAATTAGTCAAATGTGAGTTAATATTAG -3′).

Primers for the 3′ sequences were RG279 (SEQ ID NO:61) (5′-TCGCTGAATTCGATATCAAGCTTATCGATTTTTATGACTAGTTAATCAAATAAAAAGCATACAAG C-3′) and RG280 (SEQ ID NO:62) (5′-TTATCGAGCTCTGTAACATCAGTATCTAAC-3′). The primers were designed to include a multiple cloning site flanked by vaccinia transcriptional and translational termination signals. Also included at the 5′-end and 3′-end of the left arm and right arm were appropriate restriction sites (Asp718 and EcoRI for left arm and EcoRI and SacI for right arm) which enabled the two arms to ligate into Asp718/SacI digested pBS-SK plasmid vector. The resultant plasmid was designated as pC3I.

A 908 bp fragment of canarypox DNA, immediately upstream of the C3 locus was obtained by digestion of plasmid pWW5 with NsiI and SspI. A 604 bp fragment of canarypox DNA was derived by PCR (Engelke et al., 1988) using plasmid PWW5 as template and oligonucleotides CP16 (SEQ ID NO:63) (5′-TCCGGTACCGCGGCCGCAGATATTTGTTAGCTTCTGC-3′) and CP17 (SEQ ID NO:64) (5′-TCGCTCGAGTAGGATACCTACCTACTACCTACG-3′). The 604 bp fragment was digested with Asp 718 and XhoI (sites present at the 5′ ends of oligonucleotides CP16 and CP17, respectively) and cloned into Asp718-XhoI digested and alkaline phosphatase treated IBI25 (International Biotechnologies, Inc., New Haven, Conn.) generating plasmid SPC3LA. SPC3LA was digested within IBI25 with EcoRV and within canarypox DNA with NsiI and ligated to the 908 bp NsiI-SspI fragment generating SPCPLAX which contains 1444 bp of canarypox DNA upstream of the C3 locus.

A 2178 bp BglII-StyI fragment of canarypox DNA was isolated from plasmids pXX4 (which contains a 6.5 kb NsiI fragment of canarypox DNA cloned into the PstI site of pBS-SK). A 279 bp fragment of canarypox DNA was isolated by PCR (Engelke et al., 1988) using plasmid pXX4 as template and oligonucleotides CP19 (SEQ ID NO:65) (5′-TCGCTCGAGCTTTCTTGACAATAACATAG-3′) and CP20 (SEQ ID NO:66) (5′-TAGGAGCTCTTTATACTACTGGGTTACAAC-3′). The 279 bp fragment was digested with XhoI and SacI (sites present at the 5′ ends of oligonucleotides CP19 and CP20, respectively) and cloned into SacI-XhoI digested and alkaline phosphatase treated IBI25 generating plasmid SPC3RA.

To add additional unique sites to the polylinker, pC3I was digested within the polylinker region with EcoRI and ClaI, treated with alkaline phosphatase and ligated to kinased and annealed oligonucleotides CP12 (SEQ ID NO:67) (5′-AATTCCTCGAGGGATCC-3′) and CP13 (SEQ ID NO:68) (5′-CGGGATCCCTCGAGG-3′) (containing an EcoRI sticky end, XhoI site, BamHI site and a sticky end compatible with ClaI) generating plasmid SPCP3S. SPCP3S was digested within the canarypox sequences downstream of the C3 locus with StyI and SacI (pBS-SK) and ligated to a 261 bp BglII-SacI fragment from SPC3RA and the 2178 bp BglII-StyI fragment from pXX4 generating plasmid CPRAL containing 2572 bp of canarypox DNA downstream of the C3 locus. SPCP3S was digested within the canarypox sequences upstream of the C3 locus with Asp718 (in PBS-SK) and AccI and ligated to a 1436 bp Asp718-AccI fragment from SPCPLAX generating plasmid CPLAL containing 1457 bp of canarypox DNA upstream of the C3 locus. CPLAL was digested within the canarypox sequences downstream of the C3 locus with StyI and SacI (in pBS-SK) and ligated to a 2438 bp StyI-SacI fragment from CPRAL generating plasmid CP3L containing 1457 bp of canarypox DNA upstream of the C3 locus, stop codons in six reading frames, early transcription termination signal, a polylinker region, early transcription termination signal, stop codons in six reading frames, and 2572 bp of canarypox DNA downstream of the C3 locus.

The early/late H6 vaccinia virus promoter (Taylor et al., 1988a,b; Perkus et al., 1989) was derived by PCR (Engelke et al., 1988) using pRW838 (a plasmid containing the rabies glycoprotein gene (Kieny et al., 1984) linked to the H6 promoter) as template and oligonucleotides CP21 (SEQ ID NO:69) (5′-TCGGGATCCGGGTTAATTAATTAGTTATTAGACAAGGTG-3′) and CP22 (SEQ ID NO:70) (5′-TAGGAATTCCTCGAGTACGATACAAACTTAAGCGGATATCG-3′). The PCR product was digested with BamHI and EcoRI (sites present at the 5′ ends of oligonucleotides CP21 and CP22, respectively) and ligated to CP3L that was digested with BamHI and EcoRI in the polylinker generating plasmid VQH6CP3L.

ALVAC donor plasmid VQH6CP3L was digested within the polylinker with XhoI and within the H6 promoter with NruI and ligated to a NruI/HindIII fragment from 22CMVgB containing part of the H6 promoter and gB gene and a polylinker derived from pIBI24 by XhoI and HindIII digestion generating the ALVAC donor plasmid CP3LCMVgB. The DNA sequence of the CMVgB gene plus additional flanking DNA sequences in plasmid CP3LCMVgB is shown in FIGS. 11A-C (SEQ ID NO:4).

Cloning of the HCMV gB gene deleted of its transmembrane region into the NYVAC donor plasmid pSD553. Plasmid pSD553 is a vaccinia deletion/insertion plasmid of the COPAK series (rescuing virus vP866 (NYVAC), a derivative of the Copenhagen strain of vaccinia, contains a large deletion encompassing C7L and K1L; COPAK plasmids insert K1L plus a foreign gene into the ATI (A26L) insertion locus; selection on RK13 and MRC-5 cell possible.) It contains the vaccinia K1L host range gene (Gillard et al., 1986; Perkus et al., 1990) within flanking Copenhagen vaccinia arms, replacing the ATI region (ORFs A25L, A26L; Goebel et al., 1990a,b). pSD553 was constructed as follows.

Left and right vaccinia flanking arms were constructed by polymerase chain reaction (PCR) using pSD414, a pUC8-based clone of vaccinia SalI B (Goebel et al., 1990a,b) as template. The left arm was synthesized using synthetic deoxyoligonucleotides MPSYN267 (SEQ ID NO:71) (5′-GGGCTGAAGCTTGCTGGCCGCTCATTAGACAAGCGAATGAGGGAC-3′) and MPSYN268 (SEQ ID NO:72) (5′-AGATCTCCCGGGCTCGAGTAATTAATTAATTTTTATTACACCAGAAAAGACGGCTTGAGAT C-3′) as primers. The right arm was synthesized using synthetic deoxyoligonucleotides MPSYN269 (SEQ ID NO:73) (5′-TAATTACTCGAGCCCGGGAGATCTAATTTAATTTAATTTATATAACTCATTTTTTGAATATACT-3′) and MPSYN270 (SEQ ID NO:74) (5′-TATCTCGAATTCCCGCGGCTTTAAATGGACGGAACTCTTTTCCCCC-3′) as primers. The two PCR-derived DNA fragments containing the left and right arms were combined in a further PCR reaction. The resulting product was cut with EcoRI/HindIII and a 0.9 kb fragment isolated. The 0.9 kb fragment was ligated with pUC8 cut with EcoRI/HindIII, resulting in plasmid pSD541. The polylinker region located at the vaccinia ATI deletion locus was expanded as follows. pSD541 was cut with BglII/XhoI and ligated with annealed complementary synthetic oligonucleotides MPSYN333 (SEQ ID NO:75) (5′-GATCTTTTGTTAACAAAAACTAATCAGCTATCGCGAATCGATTCCCGGGGGATCCGGTACCC-3′) and MPSYN334 (SEQ ID NO:76) (5′-TCGAGGGTACCGGATCCCCCGGGAATCGATTCGCGATAGCTGATTAGTTTTTGTTAACAAA A-3′) generating plasmid pSD552. The K1L host range gene was isolated as a 1 kb BglII (partial)/HpaI fragment from plasmid pSD452 (Perkus et al., 1990). pSD552 was cut with BglII/HpaI and ligated with the K1L containing fragment, generating pSD553.

A HindIII fragment from SP131CMVgB (containing the HCMVgB gene under the control of the H6 promoter) was filled in with the klenow fragment of DNA polymerase I and ligated into plasmid pSD553 which had been SmaI digested and alkaline phosphatase treated. The resulting NYVAC donor plasmid (in which the H6 promoted gB is in the same orientation as K1L) was designated 553H6CMVgB. The DNA sequence of the CMVgB gene plus additional flanking DNA sequences in plasmid 553H6CMVgB is shown in FIGS. 12A and B (SEQ ID NO:5).

The sequence of CMVgB deleted of its transmembrane region is presented in FIG. 13 (SEQ ID NO:6). The nucleotides encoding the transmembrane region were deleted in the following manner. Oligonucleotides SPgB3 (SEQ ID NO:77) (5′-GATCCATGGACTCGACAGCGGCGTCTCTGCATGCAGCCGCTGCAGA-3′) and SPgB4 (SEQ ID NO:78) (5′-AGCTTCTGCAGCGGCTGCATGCAGAGACGCCGCTGTCGAGTCCATG-3′) were kinased, annealed and cloned into BamHI/HindIII digested and alkaline phosphatase treated IBI24 generating plasmid SPCMVgB2. Oligonucleotides SPgB1 (SEQ ID NO:79) (5′-TACGAATTCTGCAGTTCACCTATGACACGTTGC-3′) and SPgB2 (SEQ ID NO:80) (5′-ATAGGATCCATGGTCGTCCAGACCCTTGAGGTAGGGC-3′) were used in PCR with plasmid SP131CMVgB as template to generate a 0.7 kb fragment. This fragment was digested with EcoRI/BamHI and cloned into EcoRI/BamHI digested and alkaline phosphase treated IBI24 generating plasmid SPCMVgB1. A 0.7 kb EcoRI/NcoI fragment from SPCMVgB1 was ligated to EcoRI/NcoI digested and phosphatase treated SPCMVgB2 generating plasmid SPCMVgB3. The unique NcoI site in SPCMVgB3 was deleted by mutagenesis (Mandecki, 1986) using oligonucleotide SPgB5 (SEQ ID NO:81) (5′-GCCCTACCTCAAGGGTCTGGACGACACTCGACAGCGGCGTCTCTGCAT-3′) generating plasmid SPCMVgB4. A 0.7 kb PstI fragment from SPCMVgB4 was ligated to a 6.6 kb PstI fragment from 553H6CMVgB generating NYVAC donor plasmid 553H6CMVgBTM⁻. This plasmid contains the gB gene under the control of the H6 promoter with its transmembrane region deleted (amino acids 715-772; Spaete et al., 1988). The DNA sequence of the transmembrane deleted CMVgB gene plus additional flanking DNA sequences in plasmid 553H6CMVgBTM⁻ is shown in FIGS. 14A and B (SEQ ID NO:7).

Cloning the HCMVgB gene deleted of its transmembrane region and containing an altered cleavage site into NYVAC donor plasmid pSD553. The sequence of CMVgB deleted of its transmembrane region and containing an altered cleavage site is presented in FIG. 15 (SEQ ID NO:8). The alteration of the cleavage site was accomplished in the following manner. Oligonucleotides SPgB8 (SEQ ID NO:82) (5′-AATTGGTGACCG-3′) and SPgB9 (SEQ ID NO:83) (5′-GATCCGGTCACC-3′) were kinased, annealed and cloned into EcoRI/BamHI digested and alkaline phosphatase treated IBI24 generating plasmid BstIBI. A 1.4 kb BstEII/SpHI fragment from 553H6CMVgBTM⁻ was cloned into BstEII/SpHI digested and alkaline phosphatase treated BstIBI generating plasmid SPCMVgB5.

Oligonucleotides SPgB10 (SEQ ID NO:84) (5′-TGAAAGACCGAATTCTGCGT-3′) plus SPgB11 (SEQ ID NO:85) (5′-TGCGATTCATCGGTTTGTTGTAGAT-3′) and SPgB12 (SEQ ID NO:86) (5′-GACCCTTGAGGTAGGGCGGC-3′) plus SPgB13 (SEQ ID NO:87) (5′-ACTCATAATAGAACCATAAGATCTACAGATGGCAACAAT-3′) were used in PCR with plasmid 553H6CMVgBTM⁻ to generate 0.7 and 0.8 kb fragments. These two fragments were combined in a PCR with oligonucleotides SPgB10 plus SPgB12 to generate a 1.2 kb fragment. The 1.2 kb fragment was digested with EcoRI and PstI and a 0.5 kb fragment isolated and cloned into EcoRI/PstI digested and alkaline phosphatase treated IBI24 generating plasmid SPCMVgB6. The 0.5 kb EcoRI/PstI fragment from SPCMVgB6 was used to replace the corresponding fragment in SPCMVgB5 generating plasmid SPCMVgB7. A 1.4 kb BstEII/SpHI fragment from SPCMVgB7 was used to replace the corresponding fragment in 553H6CMVgB generating NYVAC donor plasmid 553H6gBC⁻TM⁻. This plasmid contains the gB gene under the control of the H6 promoter with its transmembrane region deleted (amino acids 715-772) and an alteration at the cleavage site (RTKR*ST modified to RTIRST where the asterisk indicated where cleavage normally occurs (Spaete et al., 1988) the S codon was modified to create a BglII restriction site). The DNA sequence of the cleavage site altered and transmembrane deleted CMVgB gene plus additional flanking DNA sequences in plasmid 553H6gBC⁻TM⁻ is shown in FIGS. 16A and B (SEQ ID NO:9).

Example 3.2 Construction of Recombinant Poxviruses Containing HCMVgB

Procedures for transfection of recombinant donor plasmids into tissue culture cells infected with a rescuing poxvirus and identification of recombinants by in situ hybridization on nitrocellulose filters have been described (Guo et al., 1989; Panicali and Paoletti, 1982; Piccini et al., 1987; Perkus et al., 1993). Plasmid 542CMVgB was transfected into NYVAC (vP866) infected Vero cells (ATCC CCL#81) to generate the recombinant vP1001 (NYVAC-gB). Plasmid CP3LCMVgB was transfected into ALVAC infected primary chicken embryo fibroblast (CEF) cells to generate the recombinant vCP139 (ALVAC-gB). Plasmids 553H6CMVgB, 553H6CMVgBTM⁻ and 553H6gBC⁻TM⁻ were transfected into NYVAC infected Vero cells to generate the recombinants vP1126, vP1128 and vP1145, respectively. Plasmid 22CMVgB was transfected into Vero cells infected with the WR L variant vaccinia virus (Panicali et al., 1981) to generate the recombinant vP992.

Example 3.3 Immunoprecipetation of HCMVgB Expressed by Poxvirus Recombinants

Immunoprecipitation assays were performed as described previously (Taylor et al., 1990) using gB specific guinea pig polyclonal serum (Gönczöl et al., 1990). The apparent molecular weights of the gB specific bands corresponded to previously published results (Britt and Auger, 1986; Britt and Vugler, 1989; Reis et al., 1993). The intracellular fraction from vP992, vP1001, vCP139, vP1126, vP1128 and vP1145 contained a major band of apparent molecular weight 130-140 kDa, identifiable as the glycosylated uncleaved gB precursor. Fainter bands at approximately 110 kDa and 55 kDa, representing the N-terminal and C-terminal processed fragments were also seen in the cell fractions. The extracellular medium from vP1128 and vP1145 infected cells contained the uncleaved precursor and N-terminal and C-terminal processed fragments.

Example 3.4 Humoral Response of Laboratory Animals Inoculated with ALVAC-gB and NYVAC-gB

Following a single immunization of CBA mice with vP1001 (NYVAC-gB), neutralizing antibody titers of the sera of inoculated mice were assessed (Gönczöl et al., 1986). Antibodies capable of neutralizing HCMV were detected (Table 5) in the sera of mice 14-21 days later (geometric mean titers of 1:16) and between 28-60 days post-immunization (gmt=1:26). A single immunization of CBA mice with vCP139 (ALVAC-gB) generated HCMV neutralizing antibody titers of 1:64 gmt (14-21 days pi) and 1:111 gmt (between 28 and 60 days pi). Thus, immunization of mice with NYVAC and ALVAC recombinants expressing HCMV gB elicited antibodies able to neutralize the infectivity of HCMV.

ALVAC-gB (vCP139) was evaluated for safety and immunogenicity in human volunteers. After two inoculations with 10^(6.3)TCID₅₀ of this recombinant, no serious reactions were noted.

TABLE 5 HCMV Neutralizing Antibodies in CBA mice Days After Immunization Immunization 14-21 21-28 28-60 NYVAC-gB 16 16 32 24 32 24 ALVAC-gB 32 64 128 64 64 128 128 96 Immunization was i.p. with 2-4 × 10⁸ PFU of recombinant viruses.

Guinea pigs were immunized twice with ALVAC-gB (days 0 and 28) and sera were tested for the presence of HCMV neutralizing antibody. HCMV neutralizing antibody was detected (Table 6) in the sera on day 34 (gmt=60), day 42 (gmt=60) and day 56(gmt=60). Thus, immunization of guinea pigs with ALVAC-gB elicited antibodies able to neutralize the infectivity of HCMV.

TABLE 6 HCMV Neutralizing Antibodies in Guinea Pigs Inoculated with ALVAC-gB Days Guinea Pig # 0 14 28 34 42 56 19 <4 <4 <4 64 64 64 20 <4 <4 <4 32 64 64 21 <4 <4 <4 12 32 64 22 <4 <4 <4 48 48 32 23 <4 <4  4 96 46 46 24 <4 <4 <4 46 46 32 Guinea pigs were inoculated by intramuscular route on days 0 and 28 with 10⁶³ TCID₅₀

Example 3.5 Cloning of HCMVgH in Poxvirus Vectors

Cloning of the HCMVgH gene into the NYVAC donor plasmid pSD550. The HCMVgH gene was isolated from genomic DNA (Towne strain) by PCR using oligonucleotides SPgH1 (SEQ ID NO:87) (5′-TATCTGCAGATGCGGCCAGGCCTCCCCTCCTAC-3′) and SPgH2 (SEQ ID NO:88) (5′-CCGAAGCTTTCAGCATGTCTTGAGCATGC-3′). The resulting 2.3 kb fragment was digested with PstI (site at the 5′ end of SPgH1) and HindIII (site at the 5′ end of SPgH2) and cloned into PstI/HindIII digested and alkaline phosphatase treated IBI24 generating plasmid SPgH1. The sequence of CMVgH is presented in FIG. 17 (SEQ ID NO:10).

The 3′ end of the gH gene in SPgH1 was modified to contain a vaccinia virus early transcription termination signal (Yuen and Moss, 1987) and a unique XhoI restriction site in the following manner. SPgH1 was digested within the 3′ end of the gH gene with SpHI and within IBI24 with HindIII and the fragment containing gH was purified and ligated to kinased and annealed oligonucleotides SPgH16 (SEQ ID NO:89) (5′-CTCAAGACATGCTGATTTTTATCTCGAGA-3′) and SPgH17 (SEQ ID NO:90) (5′-AGCTTCTCGAGATAAAAATCAGCATGTCTTGAGCATG-3′) generating plasmid SPgH2.

Kinased and annealed oligonucleotides SPgH12 (SEQ ID NO:91) (5′-AATTCTCGAGTTTATTGGGAAGAATATGATAATATTTTGGGATTTC-3′), SPgH13 (SEQ ID NO:92) (5′-AAAATTGAAAATATATAATTACAATATAAAATGCGGCCCGGG-3′), SPgH14 (SEQ ID NO:93) (5′-GATCCCCGGGCCGCATTTTATATTGTAATTATAT-3′) and SPgH15 (SEQ ID NO:94) (5′-ATTTTCAATTTTGAAATCCCAAAATATTATCATATTCTTCCCAATAAACTCGAG-3″) were ligated to EcoRI/BamHI digested and alkaline phosphatase treated IBI24 generating plasmid SPgH3 which contains a unique XhoI site, the entomopox 42K promoter and nucleotide sequences encoding the first four amino acids of HCMVgH (underlined bases in codons three and four in oligonucleotides SPgH13 (SEQ ID NO:92) and SPgH14 (SEQ ID NO:93) were modified to create a SmaI site without altering the amino acid sequence). Oligonucleotides SPgH18 (SEQ ID NO:95) (5′-TTAGAATTCCCCGGGCTCCCCTCCTACCTCATCGT-3′) and SPgH19 (SEQ ID NO:96) (5′-TTACTGCAGTAAGTGTTAAGTCTCTGTTGGTATC-3′) were used in PCR with plasmid SPgH1 as template to derive a 0.4 kb fragment. This fragment was digested with SmaI and PstI and cloned into SmaI/PstI digested and alkaline phosphatase treated SPgH3 generating plasmid SPgH5 which contains a unique XhoI site, the 42K promoter and 5′ 15% of the HCMVgH gene. A 0.4 kb EcoRI/BglII fragment from SPgH5 was ligated to a 4.7 kb EcoRI/BglII fragment from SPgH3 generating plasmid SPgH6 which contains the 42K promoted gH gene flanked by XhoI sites.

Plasmid pSD550 (an I4L locus donor plasmid) was derived from plasmid pSD548 (Tartaglia et al., 1992). The polylinker region in pSD548 was modified by cutting with BglII and SmaI and ligating to annealed synthetic oligonucleotides 539A (SEQ ID NO:97) (5′-AGAAAAATCAGTTAGCTAAGATCTCCCGGGCTCGAGGGTACCGGATCCTGATTAGTTAATTTTTGT-3′) and 539B (SEQ ID NO:98) (5′-GATCACAAAAATTAACTAATCAGGATCCGGTACCCTCGAGCCCGGGAGATCTTAGCTAACTGATTTTTCT-3′) resulting in plasmid pSD550. The 2.3 kb XhoI fragment from SPgH6 was cloned into XhoI digested and alkaline phosphatase treated pSD550 generating the NYVAC donor plasmid I4L42KgH in which the orientation of gH is in the same direction as the replaced I4L gene. The DNA sequence of CMVgH plus additional flanking DNA sequences in plasmid I4L42KgH are shown in FIGS. 18A and B (SEQ ID NO:11).

Cloning of the HCMVgH gene into the ALVAC donor plasmid NVOC5LSP. A C5 insertion vector containing 1535 bp upstream of C5, polylinker containing KpnI/SmaI/XbaI and NotI sites and 404 bp of canarypox DNA (31 base pairs of C5 coding sequence and 373 bp of downstream sequence) was derived in the following manner. A genomic library of canarypox DNA was constructed in the cosmid vector puK102 (Knauf and Nester, 1982) probed with pRW764.5 (a PuC9 based plasmid containing an 880 bp canarypox PvuII fragment which includes the C5 ORF Nucleotides 1372 to 2251 in FIG. 65 (SEQ ID NO:43)) and a clone containing a 29 kb insert identified (pHCOS1). A 3.3 kb ClaI fragment from pHCOS1 containing the C5 region was identified. The C5 open reading frame is initiated at position 1537 and terminated at position 1857 in the sequence shown in FIG. 65 (SEQ ID NO:43).

The C5 insertion vector was constructed in two steps. The 1535 bp upstream sequence was generated by PCR amplification using oligonucleotides C5A (SEQ ID NO:99) (5′-ATCATCGAATTCTGAATGTTAAATGTTATACTTTG-3′) and C5B (SEQ ID NO:100) (5′-GGGGGTACCTTTGAGAGTACCACTTCAG-3′) and purified genomic canarypox DNA as template. This fragment was digested with EcoRI (within oligoC5A) and cloned into EcoRI/SmaI digested pUC8 generating C5LAB. The 404 bp arm was generated by PCR amplification using oligonucleotides C5C (SEQ ID NO:101) (5′-GGGTCTAGAGCGGCCGCTTATAAAGATCTAAAATGCATAATTTC-3′) and C5DA (SEQ ID NO:102) (5′-ATCATCCTGCAGGTATTCTAAACTAGGAATAGATG-3′). This fragment was digested with PstI (within oligoC5DA) and cloned into SmaI/PstI digested C5LAB generating pC5L.

pC5L was digested within the polylinker with Asp718 and NotI, treated with alkaline phosphatase and ligated to kinased and annealed oligonucleotides CP26 (SEQ ID NO:103) (5′-GTACGTGACTAATTAGCTATAAAAAGGATCCGGTACCCTCGAGTCTAGAATCGATCCCGGGTTTTTATGA CTAGTTAATCAC-3′) and CP27 (SEQ ID NO:104) (5′-GGCCGTGATTAACTAGTCATAAAAACCCGGGATCGATTCTAGACTCGAGGGTACCGGATCCTTTTTATAGCTAATTAGTCAC-3′) (containing a disabled Asp 718 site, translation stop codons in six reading frames, vaccinia early transcription termination signal (Yuen and Moss, 1987), BamHI KpnI XhoI XbaI ClaI and SmaI restriction sites, vaccinia early transcription termination signal, translation stop codons in six reading frames, and a disabled NotI site) generating plasmid C5LSP. The polylinker region in C5LSP was further modified by digesting with BamHI and ligating to annealed oligonucleotides CP32 (SEQ ID NO:105) (5′-GATCTTAATTAATTAGTCATCAGGCAGGGCGAGAACGAGACTATCTGCTCGTTAATTAATTAGGTCGACG-3′) and CP33 (SEQ ID NO:106) (5′-GATCCGTCGACCTAATTAATTAACGAGCAGATAGTCTCGTTCTCGCCCTGCCTGATGACTAATTAATTAA-3′) generating plasmid VQC5LSP. VQC5LSP was digested with EcoRI, treated with alkaline phosphatase, ligated with kinased and annealed oligonucleotide CP29 (SEQ ID NO:107) (5′-AATTGCGGCCGC-3′) and digested with NotI. The linearized plasmid was purified and self ligated to generate plasmid NVQC5LSP. The 2.3 kb XhoI fragment from SPgH6 was cloned into XhoI digested and alkaline phosphatase treated NVQC5LSP generating the ALVAC donor plasmid NVQC5L42KgH in which the orientation of gH is in the same direction as the deleted C5 gene. The DNA sequence of CMVgH plus additional flanking DNA sequences in plasmid NVQC5L42KgH are shown in FIGS. 19A and B (SEQ ID NO:12).

Cloning of the HCMVgH gene into the vaccinia donor plasmid pSD157K1LINS. Plasmid pHK (which contains the WR vaccinia HindIII K fragment cloned in pBR322) was digested with HindIII/BglII and a 1.2 kb fragment isolated and cloned into BamHI/HindIII digested pBS-SK⁺ yielding plasmid pBS-HKARM. pBS-HKARM was digested with Asp718 in the polylinker region, blunt ended with the klenow fragment of E. Coli DNA polymerase, and digested with HindIII at the pBS/vaccinia junction. The resulting 4.1 kb vector fragment was ligated to a 2.0 kb NruI/HindIII fragment from pHM-1 (pHM-1 contains the WR vaccinia virus HindIII M fragment cloned in pBR322) resulting in plasmid pMPWRMK. pMPWRMK was cut with HpaI and ligated with annealed synthetic oligonucleotides MPSYN527 (SEQ ID NO:108) (5′-ATAAAAATTAGCTACTCAGGTACCCTGCAGTCGCGAGGATCCGAATTCCCCGGGCTCGAGTGATTAATTAGTTTTTAT-3′) and MPSYN528 (SEQ ID NO:109) (5′-ATAAAAACTAATTAATCACTCGAGCCCGGGGAATTCGGATCCTCGCGACTGCAGGGTACCTGAGTAGCTAATTTTTAT-3′). The resulting plasmid is pSD157K1LINS. pSD157K1LINS was digested within its polylinker region with XhoI, treated with alkaline phosphatase and ligated to the 2.3 kb XhoI fragment from SPgH6 yielding plasmid MP804-42KgH (which contains the HCMVgH gene and vaccinia K1L gene both in the same orientation.) The DNA sequence of CMVgH plus additional flanking DNA sequences in plasmid MP804-42KgH are shown in FIG. 20 (SEQ ID NO:13).

Example 3.6 Construction of Recombinant Poxviruses Containing HCMVgH

Plasmid I4L42kgH was transfected into NYVAC infected CEF cells to generate the recombinant vP1173 (containing HCMVgH). The same plasmid was transfected into vP1001 infected Vero cells to generate the recombinant vP1183 (containing HCMVgB and gH).

Plasmid NVQC5L42KgH was transfected into ALVAC infected CEF cells to generate the recombinant vCP236 (containing HCMVgH). The same plasmid was transfected into vCP139 infected CEF cells to generate the recombinant vCP233 (containing HCMVgB and gH). Vaccinia virus vP1170 (which contains Ecogpt under the transcriptional control of the entomopoxvirus 42K promoter in place of the deleted K1L gene) was used to infect Vero cells transfected with plasmid MP804-42KgH to generate the recombinant vP1205B.

Example 3.7 Immunoprecipitation of HCMVgH Expressed by Poxvirus Recombinants

Immunoprecipitation performed with a monoclonal antibody specific for HCMVgH demonstrated the expression of an 86 kDa gH protein (Pachl et al., 1989) by recombinants vP1173, vP1183, vP1205B, vCP233 and vCP236. Immunoprecipitation with the gB specific guinea pig polyclonal serum demonstrated correct expression of gB by recombinants vP1183 and vCP233.

The HCMV 72-kDa immediate early 1 protein (IE1) is a target for CD8⁺ cytotoxic T cells in humans (Borysiewicz et al., 1988) and is recognized by CD4⁺ T cells (Alp et al., 1991). For one individual the peptide specificities of proliferative and MHC-class I-restricted cytotoxic determinants on IE1 were determined and found to be spatially distinct segments of the exon 4 coding region (Alp et al., 1991).

The IE1 protein has been shown to up-regulate expression from its own promoter (Cherrington and Mocarski, 1989) as well as expression from the HIV LTR (Biegalke and Geballe, 1991; Ghazal et al., 1991) and expression of the promoters for the cellular genes c-myc, c-fos and hsp70 (Hagemeier et al., 1992; Santomenna and Colberg-Poley, 1990; Colberg-Poley et al., 1992). Lafemina et al., (1989) reported that the IE1 protein expressed in stable cell lines preferentially associates with metaphase chromosomes and proposed that this protein may be involved in maintenance of a putative plasmid state for HCMV DNA during latency.

In the following Examples 3.8 to 3.19, the development of poxvirus recombinants expressing the entire IE1 gene, IE1 deleted of amino acids 2-32, IE1 deleted of amino acids 292-319 or the exon 4 segment of IE1 are provided. These studies were performed in order to develop a form of the IE1 gene product that would be incapable of translocation to the nucleus, thus decreasing its potential to act as a transactivator, while maintaining its ability to be recognized by CD8⁺ cytotoxic T cells. Example 3.34 demonstrates that an ALVAC recombinant expressing an altered form of the IE1 protein (deleted of amino acids 2-32) which unlike the full length gene product is found in both the nucleus and cytoplasm of infected cells, can re-stimulate cytotoxic effector cells from HCMV seropositive individuals.

Example 3.8 Cloning of the Entire HCMV IE1 Gene in Poxvirus Vectors

Cloning of the HCMV IE1 gene into the vaccinia donor plasmid pSD22-H. The entire HCMV IE1 gene (AD169 strain) was derived as a 1.5 kb fragment by PCR using plasmid pJD083 as template (Akrigg et al., 1985) along with oligonucleotides IE3 (SEQ ID NO:110) (5′-ACGGATCCATAAAAATTACTGGTCAGCCTTGCTTC-3′) and IE5 (SEQ ID NO:111) (5′-ATCCGTTAAGTTTGTATCGTAATGGAGTCCTCTGCCAAGAGA-3′). The DNA sequence of CMV IE1 is presented in FIG. 21 (SEQ ID NO:14). Plasmid pSD486H6340 (which contains an irrelevant gene linked precisely to H6 promoter) was digested (within the H6 promoter) with NruI and (at the 3′ end of the irrelevant gene) with BamHI and ligated to the BamHI digested 1.5 kb PCR fragment (BamHI site located at the 5′ end of oligonucleotide IE3) generating plasmid pSD486H6HCMVIE1.

The H6 promoted IE1 gene was obtained from pSD486H6HCMVIE1 as a 1.6 kb fragment by digestion with BamHI followed by partial BglII digestion and ligated to BamHI digested pSD22-H yielding plasmid pSD22-HCMVIE1. The DNA sequence of CMV IE1 plus additional flanking DNA sequences in plasmid pSD22-HCMVIE1 are shown in FIG. 22 (SEQ ID NO:15).

Cloning of the HCMVIE1 gene into the vaccinia donor plasmid pSD554. Oligonucleotides SPIE1 (SEQ ID NO:112) (5′-CGCGAATTCTCGCGATATCCGTTAAGTTTGTATCGTAATGGAGT-3′) and SPIE2 (SEQ ID NO:113) (5′-GCCTCTAGAGTTAACCTCCTTCCTCAACAT-3′) were used in PCR with plasmid pSD486H6HCMVIE1 as template to generate a 181 bp fragment. This fragment was digested with EcoRI and XbaI and cloned into EcoRI/XbaI digested and alkaline phosphatase treated IBI24 generating plasmid SPIE1 containing part of the H6 promoter and the first 135 bp of the IE1 gene. Oligonucleotides SPIE3 (SEQ ID NO:114) (5′-CGGTCTAGAGGTTATCAGTGTAATGAAGC-3′) and SPIE4 (SEQ ID NO:115) (5′-CCGAAGCTTCTCGAGATAAAAATTACTGGTCAGCCTTGCTTCTAGT-3′) were used in PCR with plasmid pSD486H6HCMVIE1 as template to generate a 506 bp fragment. This fragment was digested with XbaI and HindIII and cloned into XbaI/HindIII digested and alkaline phosphatase treated IBI24 generating plasmid SPIE2 containing the 3′ end of the IE1 gene, a vaccinia early transcription termination signal and an XhoI site. SPIE1 was digested at the 3′ end of the inserted fragment of the IE1 gene with HindII and within the IBI24 polylinker with HindIII, alkaline phosphatase treated and ligated to a 903 bp HindII-BglII fragment from pSD486H6HCMVIE1 and a 464 bp BglII-HindIII fragment from SPIE2 generating plasmid SPIE3 containing the entire IE1 gene linked to part of the H6 promoter.

Plasmid pSD553 was cut with NruI and ligated with a SmaI/NruI fragment containing the synthetic H6 promoter (Perkus et al., 1989) upstream from the NruI site located at −26 relative to the translation initiation codon. The resulting plasmid, pMP553H6, was digested with NruI and BamHI and ligated to annealed oligonucleotides MPSYN347 (SEQ ID NO:116) (5′-CGATATCCGTTAAGTTTGTATCGTAATCTGCAGCCCGGGGGGG-3′) and MPSYN348 (SEQ ID NO:117) (5′-GATCCCCCGGGCTGCAGATTACGATACAAACTTAACGGATATCG-3′). The resulting plasmid, pSD554, contains the entire H6 promoter region through nucleotide −1 relative to the initiation codon, followed by a polylinker region. pSD554 was digested with NruI and XhoI and ligated to a 1.5 kb NruI/XhoI fragment from SPIE3 generating plasmid COPAKH6IE. The DNA sequence of CMV IE1 plus flanking DNA sequences in plasmid COPAKH6IE are shown in FIGS. 23A and B (SEQ ID NO:16).

Example 3.9 Construction of Recombinant Poxviruses Containing the Entire HCMVIE1 Gene

Plasmid pSD22-HCMVIE1 was transfected into Vero cells infected with the WR L variant to generate the recombinant vP893. Plasmid COPAKH6IE was transfected into NYVAC infected Vero cells to generate the recombinant vP1161.

Example 3.10 Expression of the Entire IE1 Gene by Poxvirus Recombinants

Immunoprecipitation studies performed with a monoclonal antibody specific for HCMVIE1 demonstrated the expression of a 72 kDa IE1 protein (Blanton and Tevethia, 1981; Cameron and Preston, 1981) by recombinants vP893 and vP1161. Immunofluorescence studies (performed as described in Taylor et al., 1990) revealed nuclear localization of the IE1 gene product.

Example 3.11 Cloning of the HCMVIE1 Gene (Lacking Amino Acids 292-319) Into the vaccinia Donor Plasmid

The DNA sequence of CMVIE1 lacking amino acids 292-319 is shown in FIG. 24 (SEQ ID NO:17). This deletion was made in the following manner. Plasmid SPIE3 was digested with SpeI and a 4239 bp fragment isolated (which lacks nucleotides 868-958 encoding amino acids 292-319). This fragment was self ligated generating plasmid SPIE4. A 1.4 kb NruI/XhoI fragment from SPIE4 was ligated to NruI/XhoI digested pSD554 generating plasmid COPAKH6IEN⁻. The DNA sequence of CMVIE1 lacking amino acids 292-319 plus flanking DNA sequences in plasmid COPAKH6IEN⁻ are shown in FIGS. 25A and B (SEQ ID NO:18).

Example 3.12 Construction of a Recombinant Poxvirus Containing the HCMV IE1 Gene Lacking Amino Acids 292-319

Plasmid COPAKH6IEN⁻ was transfected into NYVAC infected Vero cells to generate the recombinant vP1160.

Example 3.13 Expression of the HCMVIE1 Gene Lacking Amino Acids 292-319

Immunoprecipitation assays demonstrated the expression of a 69 kDa protein in cells infected with vP1160 consistent with the deletion of amino acids 292-319. Immunofluorescence studies revealed nuclear localization of this gene product.

Example 3.14 Cloning of the Exon 4 Segment of HCMVIE1 in Poxvirus Vectors

Cloning of the Exon 4 segment of HCMVIE1 in NYVAC donor plasmid SPI4LH6. The DNA sequence of the Exon 4 segment of HCMVIE1 is shown in FIG. 26 (SEQ ID NO:19). This segment of the gene was obtained in the following manner. Oligonucleotides SPIE5 (SEQ ID NO:118) (5′-CGCGAATTCTCGCGATATCCGTTAAGTTTGTATCGTAATGAAACAGATTAAGGTTCGAGT-3′) and SPIE6 (SEQ ID NO:119) (5′-GCCTCTAGATGCCGCCATGGCCTGACT-3′) were used in PCR with plasmid pSD486H6HCMVIE1 to generate a 0.5 kb fragment. This fragment was digested with EcoRI and XbaI and cloned into EcoRI/XbaI digested and alkaline phosphatase treated IBI24 generating plasmid SPIE5. Plasmid SPIE3 was digested with EcoRI and NcoI and a 3.6 kb fragment purified and ligated to a 0.47 kb EcoRI-NcoI fragment from SPIE5 generating plasmid SPIE6 which contains the Exon 4 segment of IE1 linked to part of the H6 promoter.

The early/late H6 vaccinia virus promoter (Guo et al., 1989; Perkus et al., 1989) was derived by PCR using PRW823 as template (a plasmid containing the H6 promoter linked to an irrelevant gene) and oligonucleotides CP30 (SEQ ID NO:120) (5′-TCGGGATCCGGGTTAATTAATTAGTCATCAGGCAGGGCG-3′) and CP31 (SEQ ID NO:121) (5′-TAGCTCGAGGGTACCTACGATACAAACTTAACGGATATCG-3′). The PCR product was digested with BamHI and XhoI (sites present at the 5′ end of CP30 and CP31, respectively) and ligated to BamHI/XhoI digested C5LSP generating plasmid VQH6C5LSP. This plasmid was used as template in PCR with oligonucleotides CP31 and RUB1 (SEQ ID NO:122) (5′-TCGGGATCCTTCTTTATTCTATACTTA-3′). The PCR product was digested with BamHI and XhoI (site present at the 5′ ends of RUB1 and CP31, respectively) and ligated to BamHI/XhoI digested pSD550 generating plasmid SPI4LH6. A 1.3 kb NruI/XhoI fragment isolated from SPIE6 was cloned into NruI/XhoI digested and alkaline phosphatase treated SPI4LH6 generating plasmid I4LH6IE-Ex4 (in which the H6 promoted IE1 Exon 4 gene is in the same orientation as the replaced I4L gene). The DNA sequence of the Exon 4 segment of HCMVIE1 plus flanking DNA sequences in plasmid I4LH6IE-Ex4 are shown in FIG. 27 (SEQ ID NO:20).

Cloning of the Exon 4 fragment of HCMVIE1 in ALVAC donor plasmid NVQH6C5LSP. Plasmid VQH6C5LSP was digested with EcoRI, treated with alkaline phosphatase, ligated with kinased and annealed oligonucleotide CP29 and digested with NotI. The linearized plasmid was purified and self ligated generating plasmid NVQH6C5LSP. The 1.3 kb NruI/XhoI fragment from SPIE6 was cloned into NruI/XhoI digested and alkaline phosphatase treated NVQH6C5LSP generating plasmid NVQH6IE-Ex4 (in which the H6 promoted IE1 Exon 4 gene is in the same orientation as the replaced C5 gene). The DNA sequence of the Exon 4 segment of HCMVIE1 plus flanking DNA sequences in plasmid NVQH6IE-Ex4 are shown in FIGS. 28A and B (SEQ ID NO:21).

Example 3.15 Construction of Recombinant Poxviruses Containing the EXON 4 Segment of IE1

Plasmid I4LH6IE-Ex4 was transfected into NYVAC infected CEF cells to generate the recombinant vP1186. Plasmid NVQH6IE-Ex4 was transfected into ALVAC infected CEF cells to generate the recombinant vCP244.

Example 3.16 Expression of the EXON 4 Segment of HCMVIE1 by Poxvirus Recombinants

Immunofluorescence experiments revealed cytoplasmic localization of the IE-Exon 4 protein expressed by recombinants vP1186 and vCP244. Immunoprecipitation experiments with a monoclonal antibody specific for IE-Exon 4 demonstrated the expression of a 60 kDa protein in cells infected with vCP244 consistent with the predicted size of the exon 4 segment. Immunoprecipitation with a polyclonal rabbit serum raised against a bacterial Exon 4 fusion protein revealed the expression of a 60 kDa protein in cells infected with vP1186 and VCP244.

Example 3.17 Cloning of the HCMVIE1 Gene (Lacking Amino Acids 2-32) in Poxvirus Vectors

Cloning of the HCMVIE1 gene (lacking amino acids 2-32) in NYVAC donor Rlasmid SPI4LH6. The DNA sequence of HCMVIE1 lacking amino acids 2-32 is shown in FIG. 29 (SEQ ID NO:22). This segment was obtained in the following manner. Oligonucleotides SPIE9 (SEQ ID NO:123) (5′-AATTCTCGCGATATCCGTTAAGTTTGTATCGTAATGACGACGTTCCTGCAGACTATGTTGAGGAAGGAGGTT-3′) and SPIE10 (SEQ ID NO:124) (5′-AACCTCCTTCCTCAACATAGTCTGCAGGAACGTCGTCATTACGATACAAACTTAACGGATATCGCGAG-3′) were kinased, annealed and ligated to a 4.2 kb HindII/EcoRI digested and alkaline phosphatase treated fragment from SPIE3 generating plasmid SPIE8. A 1.4 kb NruI/XhoI fragment from SPIE8 (containing part of the H6 promoter and IE1 lacking amino acids 2-32) was ligated to NruI/XhoI digested and alkaline phosphatase treated SPI4LH6 generating plasmid I4LH6IEd32. The DNA sequence of HCMVIE1 lacking amino acids 2-32 plus flanking DNA sequences in plasmid I4LH6IEd32 are shown in FIG. 30 (SEQ ID NO:23).

Cloning of the HCMVIE1 gene (lacking amino acids 2-32) in ALVAC donor Plasmid NVQH6C5LSP. The 1.4 kb NruI/XhoI fragment from SPIE8 was cloned into NruI/XhoI digested and alkaline phosphatase treated NVQH6C5LSP generating plasmid NVQH6IEd32. The DNA sequence of HCMVIE1 lacking amino acids 2-32 plus flanking DNA sequences in plasmid NVQH6IEd32 are shown in FIGS. 31A and B (SEQ ID NO:24).

Example 3.18 Construction of Poxvirus Recombinants Containing the IE1 Gene Lacking Amino Acids 2-32

Plasmid I4LH6IEd32 was transfected into NYVAC infected CEF cells to generate the recombinant vP1201. Plasmid NVQH6IEd32 was transfected into ALVAC infected CEF cells to generate the recombinant vCP256.

Example 3.19 Expression of IE1 Lacking Amino Acids 2-32 by Poxvirus Recombinants

Immunofluorescence experiments revealed both nuclear and cytoplasmic localization of the IE1 protein lacking amino acids 2-32 by recombinants vP1201 and vCP256. Immunoprecipitation with a polyclonal rabbit serum raised against a bacterial exon 4 fusion protein revealed the expression of a 68 kDa protein in cells infected with vP1201 consistent with the predicted size.

Example 3.20 Cloning of the HCMV pp65 Gene in Poxvirus Vectors

Cloning of the HCMV pp65 aene in NYVAC donor plasmid SPHA-H6. pSD456 is a subclone of Copenhagen vaccinia DNA containing the HA gene (A56R; Goebel et al., 1990a,b) and surrounding regions. pSD456 was used as a template in PCR for synthesis of left and right vaccinia arms flanking the A56R ORF. The left arm was synthesized using oligonucleotides MPSYN279 (SEQ ID NO:125) (5′-CCCCCCGAATTCGTCGACGATTGTTCATGATGGCAAGAT-3′) and MPSYN280 (SEQ ID NO:126) (5′-CCCGGGGGATCCCTCGAGGGTACCAAGCTTAATTAATTAAATATTAGTATAAAAAGTGATTTATTTTT-3′). The right arm was synthesized using oligonucleotides MPSYN281 (SEQ ID NO:127) (5′-AAGCTTGGTACCCTCGAGGGATCCCCCGGGTAGCTAGCTAATTTTTCTTTTACGTATTATATATGTAATAAACGTTC-3′) and MSYN312 (SEQ ID NO:128) (5′-TTTTTTCTGCAGGTAAGTATTTTTAAAACTTCTAACACC-3′). The purified PCR fragments for the left and right arms were combined in a further PCR reaction. The resulting product was digested with EcoRI/HindIII. The resulting 0.9 kb fragment was cloned into EcoRI/HindIII digested pUC8 resulting in plasmid pSD544.

pSD544 was digested within its polylinker with XhoI, filled in with klenow and treated with alkaline phosphatase. Plasmid SP126 (equivalent to SP131) was digested with HindIII, treated with klenow and the H6 promoter isolated by digestion with SmaI. Ligation of the H6 promoter fragment to pSD544 generated SPHA-H6.

The HCMV pp65 gene was PCR amplified using HCMV genomic DNA as template (Towne strain) and oligonucleotides pp651 (SEQ ID NO:129) (5′-GATTATCGCGATATCCGTTAAGTTTGTATCGTAATGGCATCCGTACTGGGTCCCATTTCGGG-3′) and pp651R (SEQ ID NO:130) (5′-GCATAGGTACCGGATCCATAAAAATCAACCTCGGTGCTTTTTGGGCG-3′). The DNA sequence of CMVpp65 is shown in FIG. 32 (SEQ ID NO:32). The 1.6 kb product was digested with NruI and BamHI (site present at the 5′ end of oligonucleotides pp651 and pp651R, respectively) and cloned into NruI/BamHI digested SPHA-H6 generating plasmid CMV65.1. This plasmid contained the pp65 gene linked to the H6 promoter, however, the first 30 bp of the pp65 gene were missing.

To derive a plasmid containing the first 30 bp of the pp65 gene oligonucleotides RNApp65I (SEQ ID NO:131) (5′-TAGTTCGGATCCCCGCTCAGTCGCCTACA-3′) and pp65R4 (SEQ ID NO:132) (5′-ATCAAGGGATCCATCGAAAAAGAAGAGCG-3′) were used in PCR with genomic DNA. The resulting 1 kb fragment was digested with BamHI (BamHI sites present at the 5′ ends of both oligonucleotides) and cloned into BamHI digested IBI24 generating plasmid pp65.7. Plasmid pp65.7 was used in PCR with oligonucleotides pp651B (SEQ ID NO:133) (5′-GATTATCGCGATATCCGTTAAGTTTGTATCGTAATGGAGTCGCGCGGTCGCCGTTGTCCCG-3′) and pp65BstXI (SEQ ID NO:134) (5′-ACCTGCATCTTGGTTGC-3′) to generate a 0.5 kb fragment. This fragment was digested with NruI and BstXI (sites at the 5′ ends of oligonucleotides pp651B and pp65BstXI, respectively) and ligated to a 4.8 kb NruI/BstXI fragment of CMV65.1 generating plasmid pCMV65.2. This plasmid contains the entire pp65 gene linked precisely to the H6 promoter oriented in the same direction as the replaced HA gene. The DNA sequence of CMVpp65 plus flanking DNA sequences in plasmid pCMV65.2 are shown in FIG. 33 (SEQ ID NO:26).

Cloning of the HCMV pp65 gene in ALVAC donor plasmid pMPC616E6VQ. FIGS. 34A and B (SEQ ID NO:27) is the sequence of a 3.7 kb segment of canarypox DNA. Analysis of the sequence revealed a reading frame designate C6L initiated at position 377 and terminated at position 2254. A C6 insertion vector containing 370 bp upstream of C6, polylinker containing SmaI, PstI, XhoI and EcoRI sites, and 1156 bp of downstream sequence was derived in the following manner. The 0.4 bp upstream sequence was generated by PCR amplification of a cosmid clone derived from purified genomic canarypox DNA using oligonucleotides C6A1SG (SEQ ID NO:135) (5′-ATCATCGAGCTCGCGGCCGCCTATCAAAAGTCTTAATGAGTT-3′) and C6B1SG (SEQ ID NO:136) (5′-GAATTCCTCGAGCTGCAGCCCGGGTTTTTATAGCTAATTAGTCATTTTTTCGTAAGTAAGTATTTTATTTAA-3′). The 1.2 kb downstream arm was generated by PCR amplification of the same template using oligonucleotides C6C1SG (SEQ ID NO:137) (5′-CCCGGGCTGCAGCTCGAGGAATTCTTTTTATTGATTAACTAGTCAAATGAGTATATATAATTGAAAAAGTAA-3′) and C6D1SG (SEQ ID NO:138) (5′-GATGATGGTACCTTCATAAATACAAGTTTGATTAAACTTAAGTTG-3′). These fragments were fused by a third PCR employing gel purified 0.4 and 1.2 kb fragments as template for primers C6A1SG (SEQ ID NO:135) and C6D1SG (SEQ ID NO:138). The resulting 1.6 kb fragment was isolated from an agarose gel, digested with SacI and KpnI and ligated to similarly digested pBS generating C6 insertion plasmid pC6L.

Plasmid pMPC616E6VQ was derived by cloning a HpaI-XhoI fragment containing the H6 promoter precisely linked to an irrelevant gene into Sma-XhoI digested pC6L. pMPC616E6VQ was digested with NruI and BamHI and the 4 kb vector fragment (NruI-BamHI) and 0.6 kb C6 flanking arm fragment (BamHI-BamHI) isolated. These two fragments were combined in a ligation with a 1.7 kb NruI-BamHI fragment from pCMV65.2 (containing part of the H6 promoter linked to the p65 gene) generating plasmid CMV65C6.1 which contained a C6 flanking arm, H6 promoter and the pp65 gene but lacked the 0.6 kb C6 flanking arm. CMV65C6.1 was digested with BamHI, treated with alkaline phosphatase and ligated to the 0.6 kb C6 flanking arm generating plasmid CMV65C6.2 in which C6 flanking arms are present on both sides of the H6-pp65 insert. The DNA sequence of CMVpp65 plus flanking DNA sequences in plasmid CMV65C6.2 are shown in FIGS. 35A and B (SEQ ID NO:28).

Cloning of the HCMVpp65 gene into the vaccinia donor plasmid pSD157 K1LINS. Plasmid pCMV65.2 was digested with KpNI, treated with Mung Bean Nuclease and digested with BamHI generating a 1.7 kb fragment containing H6-pp65. PSD157K1LINS was digested with BamHI and SmaI and ligated to the 1.7 kb fragment generating plasmid CMV65.WR. The DNA sequence of CMVpp65 plus flanking DNA sequences in plasmid CMV65.WR are shown in FIG. 36 (SEQ ID NO:29).

Example 3.21 Construction of Recombinant Poxviruses Containing HCMVpp65

Plasmid pCMV65.2 was transfected into NYVAC infected Vero cells to generate the recombinant vP1184 (containing HCMVpp65), into vP1001 infected Vero cells to generate the recombinant vP1196 (containing HCMVgB and pp65) and into vP1183 infected Vero cells to generate the recombinant vP1210 (containing HCMVgB, gH and pp65).

Plasmid CMV65C6.2 was transfected into ALVAC infected CEF cells to generate the recombinant vCP260 (containing HCMVpp65).

Plasmid CMV65.WR was transfected into vP1170 infected Vero cells to generate the recombinant vP1214 (WR-pp65).

Example 3.22 Expression of HCMVpp65 by Poxvirus Recombinants

Immunoprecipitation experiments with a monoclonal antibody specific for HCMV pp65 demonstrated the expression of a 65 kDa protein (Pande et al., 1991) by recombinants vP1184, vP1214, vCP260, vP1196 and vP1210. In addition, immunoprecipitation with gB specific guinea pig polyclonal sera demonstrated correct expression of gB by recombinants vP1196 and vP1210 and immunoprecipitation with a gH specific monoclonal antibody demonstrated correct expression of gH by recombinant vP1210.

Example 3.23 Cloning of the HCMV pp150 Gene in Poxvirus Vectors

Cloning of the pp150 gene into the NYVAC donor plasmid pSD541. The DNA sequence of CMVpp150 is shown in FIG. 37 (SEQ ID NO:30). Oligonucleotides pp150.1B (SEQ ID NO:139) (5′-TTCGGATCCGGTTCTGGAGAAAAGCC-3′) and pp150R6 (SEQ ID NO:140) (5′-GCTTCCAAGCTTTCCTGAAGGGATTGTAAGCC-3′) were used in PCR with Towne genomic DNA to generate a 2 kb fragment from the 5′ end of pp150. This fragment was digested with BamHI and HindIII and cloned into BamHI/HindIII digested and alkaline phosphatase treated IBI24 generating plasmid pp150.5.

Oligonucleotides pp150.9 (SEQ ID NO:141) (5′-TTCGGATCCGGCTTTCAGTCTCGTCTCC-3′) and pp150END2 (SEQ ID NO:142) (5′-TTCGGATCCATGCAATTGCCCGCGGACAAC-3′) were used in PCR with Towne DNA to generated a 1.8 kb fragment which includes the 3′ end of the gene. This fragment was digested with BamHI and cloned into BamHI digested and alkaline phosphatase treated PUC8 yielding pp150.3.

Oligonucleotides SP150-3 (SEQ ID NO:143) (5′-TTCGAATTCGCTAGCTTTATTGGGAAGAATATGATAATATTTTGGGATTTCAAAATTGAAAATATATAATTACAATATAAAATGAGTTTGCAGTTTATC-3′) and SP150-4 (SEQ ID NO:144) (5′-TTCTCTAGATGAGCTCGTTGAACAGCAC-3′) were used in PCR with plasmid pp150.5 as template to generate a 259 bp fragment. This fragment was digested with EcoRI and XbaI and cloned into EcoRI/XbaI digested and alkaline phosphatase treated IBI24 generating plasmid 150.5MP. This plasmid contains a NheI site, 65 bp entomopoxvirus 42K promoter and bases 1-170 from the 5′ end of the pp150 gene. The underlined base in the sequence of oligonucleotide SP150-3 (position −53 of the promoter) is missing in this clone.

Oligonucleotides SP150-1 (SEQ ID NO:145) (5′-CCGAAGCTTGCTAGCAATAAAAACTATTCCTCCGTGTTCTTAAT-3′) and SP150-2 (SEQ ID NO:146) (5′-GCCTCTAGATACGTAAAGCTAAGTTATC-3′) were used in PCR with plasmid pp150.3 as template to generate a 907 bp fragment. This fragment was digested with XbaI and HindIII and cloned into XbaI/HindIII digested and alkaline phosphatase treated IBI24 yielding plasmid 150.3MP. This plasmid contains nucleotides 2273-3141 from pp150 followed by a vaccinia early transcription termination signal (T₅ATT) (Yuen and Moss, 1987) and a NheI site. pp150 nucleotide 2748 (FIG. 37; SEQ ID NO:30) in this clone is an A not a C as in pp150.3, this change is silent.

Plasmid pp150.3 was digested with SnaBI and HindIII and a 3451 bp fragment isolated. Plasmid 150.3MP was digested with SnaBI and HindIII and 873 bp fragment isolated. Ligation of these two fragments yielded plasmid 150.3MC which contains pp150 nucleotides 1473-3141 followed by T₅ATT and a NheI site.

Plasmid 150.5MP was digested with SacI and HindIII and a 3056 bp fragment isolated. Plasmid pp150.5 was digested with SacI and HindIII and a 1816 bp fragment isolated. Ligation of these two fragments yielded plasmid 150.5MC which contains a NheI site, 65 bp 42K promoter and pp150 nucleotides 1-1981.

Plasmid 150.5MC was digested with HpaI and HindIII and a 4634 bp fragment isolated. Plasmid 150.3MC was digested with HaI and HindIII and a 1412 bp fragment isolated. Ligation of these two fragments yielded plasmid 150.1 which contains a NheI site, 65 bp 42K promoter, nucleotides 1-3141 pp150, T₅ATT and a NheI site.

Plasmid pSD541 is a vaccinia insertion plasmid which is deleted for vaccinia sequences encompassing the A25L and A26L ORFS (Goebel et al., 1990a,b). The deletion junction consists of a polylinker region containing XhoI, SmaI and BglII restriction sites, flanked on both sides by stop codons and early vaccinia transcriptional terminators (Yuen and Moss, 1987). pSD541 was constructed by polymerase chain reaction (PCR) using cloned vaccinia SalI E plasmid pSD414 as template. Synthetic oligonucleotides MPSYN267 (SEQ ID NO:71) (5′-GGGCTCAAGCTTGCGGCCGCTCATTAGACAAGCGAATGAGGGAC-3′) and MPSYN268 (SEQ ID NO:72) (5′-AGATCTCCCGGGCTCGAGTAATTAATTAATTTTTATTACACCAGAAAAGACGGCTTGAGATC-3′) were used as primers to generate the left vaccinia arm and synthetic oligonucleotides MPSYN269 (SEQ ID NO:73) (5′-TAATTACTCGAGCCCGGGAGATCTAATTTAATTTAATTTATATAACTCATTTTTTGAATATACT-3′) and MPSYN270 (SEQ ID NO:74) (5′-TATCTCGAATTCCCGCGGCTTTAAATGGACGGAACTCTTTTCCCC-3′) were used to generate the right vaccinia arm. PCR products consisting of the left and right vaccinia arms were combined, and subjected to PCR amplification. The PCR product was digested with EcoRI and HindIII and electrophoresed on a agarose gel. The 0.8 kb fragment was isolated and ligated into pUC8 cut with EcoRI/HindIII, resulting in plasmid pSD541.

Plasmid pSD541 was digested in its polylinker region with SmaI and alkaline phosphatase treated. Plasmid 150.1 was digested with NheI, treated with klenow and a 3224 bp fragment (containing 42K-pp150) isolated. Ligation of these two fragments yielded plasmid 150.7. The DNA sequence of CMVpp150 plus flanking DNA sequences in plasmid 150.7 are shown in FIGS. 38A and B (SEQ ID NO:31).

Cloning of the pp150 gene into ALVAC donor plasmid PMM117. Plasmid PMM117 is a derivative of pC6L with a modified polylinker region. PMM117 was digested in its polylinker with EcoRI filled in with klenow and treated with alkaline phosphatase. Plasmid 150.1 was digested with NheI, treated with klenow and a 3224 bp fragment (containing 42K-pp150) isolated. Ligation of these two fragments generated plasmid 150.6. The DNA sequence of CMVpp150 plus flanking DNA sequences in plasmid 150.6 are shown in FIGS. 39A and B (SEQ ID NO:32).

Cloning of the pp150 gene into vaccinia donor plasmid pSD157K1LINS. Plasmid pSD1571LINS was digested in its polylinker region with SmaI and alkaline phosphatase treated. Plasmid 150.1 was digested with NheI, treated with klenow and a 3224 bp fragment (containing 42K-pp150) isolated. Ligation of these two fragments generated plasmid 150.4. The DNA sequence of CMVpp150 plus flanking DNA sequences in plasmid 150.4 are shown in FIGS. 40A and B (SEQ ID NO:33).

Example 3.24 Construction of Recombinant Poxviruses Containing HCMVMpp150

Plasmid 150.4 was transfected into vP1170 infected CEF cells to generate the recombinant vP1238 (WR-pp150).

Plasmid 150.7 was transfected into NYVAC infected CEF cells to generate the recombinant vP1247 (NYVAC-pp150).

Plasmid 150.6 was transfected into ALVAC infected CEF cells to generate the recombinant vCP284 (ALVAC-pp150).

Example 3.25 Expression of HCMVpp150 by Poxvirus Recombinants

Western blot (Harlow and Lane, 1988) with a monoclonal antibody specific for HCMVpp150 demonstrated the expression of a 150 kDa protein in cells infected with vP1238 which comigrated with a protein present in HCMV infected cells. Expression of a 150 kDa protein was observed in vP1247 and vCP284 infected cells by immunoprecipitation with the pp150 specific monoclonal antibody.

Example 3.26 Developing a NYVAC Donor Plasmid Containing the HCMVgH and IE1 Exon 4 Genes

Plasmid I4LH6IE-Ex4 was linearized with BamHI, filled in with klenow and treated with alkaline phosphatase yielding a 4.9 kb fragment. Plasmid gH6-3 was digested with XhoI, filled in with klenow and a 2.3 kb fragment (containing 42K-gH) isolated. These two fragments were ligated to generate plasmid I4L42KgHH6IE-Ex4. The DNA sequence of CMVgH and IE-Exon4 plus additional flanking sequences in plasmid I4L42KgHH6IE-Ex4 are shown in FIGS. 41A and B (SEQ ID NO:34).

Example 3.27 Construction of NYVAC Recombinants Containing HCKVgB.+gH.+pp65.+IE-Exon 4, HCMVgB.+gh.+pp65.+pp150 OR HCMVgB.+gH.+pp65.+IE-Exon 4 and pp150

Plasmid I4L42KgHH6IE-Ex 4 was transfected into vP1196 infected Vero cells to generate the recombinant vP1216 (containing HCMVgB, gH, pp65, IE-Exon 4). Plasmid 150.7 was transfected into vP1216 infected CEF cells to generate the recombinant vP1251 (containing HCMVgB, gH, IE-Exon 4, pp65, pp150). Plasmid 150.7 was transfected into vP1210 infected Vero cells to generate the recombinant vP1262 (containing HCMV-gB, gH, pp65, pp150).

Example 3.28 Expression of the HCMV Genes in vP1216, vP1251. vP1262

Immunoprecipitation with monoclonal antibodies specific for gB, gH, pp65 and IE-Exon 4 demonstrated the correct expression of all four genes by recombinant vP1216. Immunoprecipitation with monoclonal antibodies specific for gB, gH, pp65 and IE-Exon 4 demonstrated the correct expression of these four genes by recombinant vP1251. Immunoprecipitation with monoclonal antibodies specific for gB, gH and pp65 demonstrated the correct expression of these three genes by recombinant vP1262. Western blot with a monoclonal antibody specific for ppl50 demonstrated the correct expression of this gene by recombinants vP1251 and vP1262.

Example 3.29 Developing an ALVAC Donor Plasmid Containing the HCMV pp65 and pp150 Genes

Plasmid CMV65C6.2 was linearized with EcoRI, filled in with klenow and treated with alkaline phosphatase generating a 6.3 kb fragment. Plasmid 150.1 was digested with NheI, filled in with klenow and a 3.2 kb fragment (42K-pp150) isolated. Ligation of these two fragments yielded plasmid 150.8. The DNA sequence of CMVpp65 and pp150 plus additional flanking sequences in plasmid 150.8 are shown in FIGS. 42A to C (SEQ ID NO:35).

Example 3.30 Construction of an ALVAC Recombinant Containing HCMVgB, gH, pp65 and pp150

Plasmid 150.8 was transfected into vPC233 infected CEF cells to generate an ALVAC-gB, gH, pp65, pp150 recombinant (vCP280).

Example 3.31 Expression of the HCMV Genes in vCP280

Immunoprecipitation with monoclonal antibodies specific for gB, gH and pp65 demonstrated the correct expression of these three genes by recombinant vCP280.

Example 3.32 Cloning of HCMVgL in Poxvirus Vectors Deriving a NYVAC Donor Plasmid Containing gB and gL

Oligonucleotides UL115A (SEQ ID NO:147) (5′-GCCTCTAGAATGTGCCGCCGCCCGGATTGC-3′) and UL115B (SEQ ID NO:148) (5′-CGCAAGCTTAGCGAGCATCCACTGCTTGAGGGC-3′) were used in PCR with Towne DNA as template to generate a 853 bp fragment. This fragment was digested with XbaI and HindIII and cloned into XbaI/HindIII digested and alkaline phosphatase treated IBI24 generating plasmid UL115.1. The sequence of CMVgL is presented in FIG. 43 (SEQ ID NO:65).

Oligonucleotides UL115M (SEQ ID NO:149) (5′-TCCAAGCTTAGATCTATAAAAATTAGCGAGCATCCACTGCTTGAGGGCCATAGC-3′) and UL115N (SEQ ID NO:150) (5,′-GCCTCTAGATGCTGACGCTGTTGAGCTCGGAC-3′) were used in PCR with plasmid UL115.1 as template to generate a 498 bp fragment. This fragment was digested with HindIII and XbaI and cloned into HindIII/XbaI digested and alkaline phosphatase treated IBI24 generating plasmid UL115.2.

Oligonucleotides UL115G2 (SEQ ID NO:151) (5′-CGCGAATTCTCGCGATATCCGTTAAGTTTGTATCGTAATGTGCCGCCGCCCGGATTGC-3′) and UL115H2 (SEQ ID NO:152) (5′-GCCTCTAGATTCCAGCGCGGCGCTGTGTCCGAGC-3′) were used in PCR with plasmid UL115.1 as template to generate a 450 bp fragment. This fragment was digested with EcoRI and XbaI and cloned into EcoRI/XbaI digested and alkaline phosphatase treated IBI24 generating plasmid UL115.3.

Plasmid UL115.3 was digested with HindIII and SacI and a 3226 bp fragment isolated. Plasmid UL115.2 was digested with HindIII and SacI and a 469 bp fragment isolated. Ligation of these two fragments yielded plasmid UL115.4.

Plasmid UL115.4 was digested with NruI and BglII and a 865 bp fragment isolated. Plasmid I4LH6 was digested with NruI and BglII and a 3683 bp fragment isolated. Ligation of these two fragments yielded plasmid I4LH6gL.

To correct a one base deletion in the H6 promoter in I4LH6gL this plasmid was digested with EcoRV treated with alkaline phosphatase and a 3805 bp fragment isolated. Plasmid I4LH6 was digested with EcoRV and a 736 bp fragment isolated. Ligation of these two fragments yielded plasmid I4LH6CgL.

Plasmid 542CMVgB was linearized with BamHI and treated with alkaline phosphatase. Plasmid I4LH6CgL was digested with BamHI and BalII and a 968 bp fragment (containing the H6 promoted gL gene) isolated. Ligation of these two fragments generated plasmid 542CMVgBgL. The DNA sequence of CMVgL and CMVgB plus additional flanking DNA sequences in plasmid 542CMVgBgL are shown in FIGS. 44A and B (SEQ ID NO:37).

Example 3.33 Developing a NYVAC Recombinant Containing gB, gH, gL, pp65, pp150, IE1-Exon 4 or gB, gH, gL, pp65, pp150

Plasmid 542CMVgBgL was transfected into vP1251 infected CEF cells to generate a NYVAC gB, gH, gL, pp65, pp150, IE1-Exon 4 recombinants (NYVAC-CMV6: vP1302 and vP1302B).

Plasmid 542CMVgBgL is transfected into vP1262 infected cells to generate NYVAC recombinant vP1312 (NYVAC-CMV5).

Example 3.34 Human Cytotoxic T Lymphocyte Responses to HCMV Proteins

Lymphocytes comprising the antigen-specific segment of the immune system may functionally react to antigen by producing antibodies (B-lymphocytes) or by becoming cytotoxic T lymphocytes (CD8+ T-lymphocytes). ALVAC recombinants expressing HCMV proteins that are known to be recognized by human cytotoxic T lymphocytes (CTLs) are capable of re-stimulating human cellular immune responses with characteristics of classical CTLs.

Thirteen individuals for which there was previously established EBV-transformed B-cell lines (LBCL) for use as CTL targets were screened for CTL responses to HCMV gB, IE1, and pp65. Although only one of these volunteer blood donors had an established clinical history of HCMV infection, seven were found to be HCMV seropositive by virtue of their sera containing antibodies which neutralized HCMV.

Stimulation of HCMV 1E1 CTLs by ALVAC-1E1 (vCP256): Whole blood was collected into heparinized Vacutainer tubes from each volunteer donor by venipuncture. The mononuclear cell fraction was separated from the remainder of the blood components by centrifugation over Leucoprep gradients, washed several times by centrifugation in Stim Medium (MEM containing 5% fetal bovine serum [FBS], 2 mM L-glutamine, 10⁻⁴ M 2-mercaptoethanol, 100 IU/ml penicillin, and 100 μg/ml streptomycin), counted for viable cells with trypan blue, and resuspended at 5×10⁶ cells/ml in Stim Medium (responder cells). A portion of the mononuclear cells were resuspended at 10⁷ cells/ml in MEM containing 2% FBS and infected with recombinant ALVAC expressing HCMV 1E1 (vCP256) at a multiplicity of infection of 25 for approximately 1 hour at 37 C. Following incubation, sufficient Stim Medium was added to dilute the infected cells to 5×10⁵ cells/ml (stimulator cells). Equal volumes of responder cells and stimulator cells were added to upright 25 cm² tissue culture flasks or to the wells of 24-well tissue culture plates and incubated in 5% CO₂/95% air at 37° C. for 6 days. Target cells were prepared by infecting LBCLs with recombinant WR vaccinia virus expressing HCMV 1E1 (vP893) similarly to the infection of stimulator cells except the target cells were incubated overnight at 4×10⁵ cells/ml in RPMI 1640 medium containing 20% FBS. Following incubation, the mononuclear cells and the target cells were washed by centrifugation in Assay Medium (RPMI 1640 medium containing 10% FBS, 2 mM L-glutamine, 5×10⁻⁵ M 2-mercaptoethanol, 100 IU/ml penicillin, and 100 μg/ml streptomycin). Target cells were incubated in Na₂ ⁵¹CrO₄ for 1 hour, washed by centrifugation in Assay Medium, resuspended to 10⁵ cells/ml in Assay Medium, and held on ice until use. Following centrifugation, the mononuclear cells were diluted to 2×10⁶ cells/ml in Assay Medium. One tenth ml of mononuclear cells and 0.1 ml of ⁵¹Cr labelled, infected target cells were added to the wells of 96-well round bottom tissue culture plates. These volumes and cell densities resulted in an effector to target ratio (E:T) of 20:1. The tissue culture plates were centrifuged at 250 g for 2 minutes and incubated in 5% CO₂/95% air at 37 C. for 4 to 5 hours. Following incubation, 0.1 ml of supernatant fluid from each well was collected using Skatron filter wicks and counted for released radioactivity. Percent cytoxicity was calculated as:

 (EXPERIMENTAL ⁵¹CR RELEASE−SPONTANEOUS ⁵¹CR RELEASE)/(MAXIMUM ⁵¹CR RELEASE−SPONTANEOUS ⁵¹CR RELEASE)×100.

Maximum release was determined by the addition of 5% sodium dodecyl sulfate to target cells while spontaneous release was determined by incubating target cells in the absence of effector cells. In none of the experiments presented did spontaneous release of ⁵¹Cr from target cells exceed 20% of maximum ⁵¹Cr release.

Following in vitro stimulation with ALVAC recombinants expressing a single HCMV protein, mononuclear cells from four of the seven seropositive volunteer donors lysed autologous targets expressing HCMV IE1 (FIG. 45) and mononuclear cells from six of the seven seropositive donors lysed autologous targets expressing HCMV pp65 (FIG. 46). Re-stimulated mononuclear cells from none of the HCMV seropositive donors lysed autologous targets expressing HCMV gB.

The mononuclear cells from HCMV seronegative volunteer donors, when re-stimulated similarly to the mononuclear cells of the HCMV seropositive donors, failed to lyse autologous target cells expressing HCMV IE1 or HCMV pp65 (FIG. 45 and FIG. 46, respectively).

In all cases except one, the cytotoxic effector cells only lysed autologous, but not nonautologous, target cells expressing the appropriate HCMV protein. The single exception, mononuclear cells from Donor 7C, following re-stimulation with ALVAC pp65 (vCP260), was capable of lysing nonautologous target cells expressing HCMV pp65. However, it was later demonstrated that Donor 7C and the donor for the nonautologous target cell line share HLA-B7 of the human major histocompatibility complex (MHC).

Stimulation of HCMV IE1 CTLs by ALVAC-IE1 (vCP256): Human CTLs were stimulated in vitro and assayed for HCMV IE1 CTLs using similar methodology as in FIG. 45 except that following 6 days incubation for restimulation, the responder mononuclear cells were incubated with immunomagnetic beads coupled to monoclonal anti-human CD3, CD4, or CD8. Following incubation, the beads were removed by a magnet and therefore the CD3+, CD4+ or CD8+ cells. The cells adhering to the magnetic beads were uncoupled, washed and used in the cytotoxicity assay.

Representative of the phenotype of the cytotoxic responses of this HCMV seropositive cohort, the ALVAC-IE1 (vCP256) re-stimulated mononuclear cells from Donor 2A failed to lyse IE1-expressing targets following depletion of lymphocytes expressing CD3 and CD8, but not CD4 (FIG. 47). Furthermore, re-stimulated mononuclear cells that had been enriched for CD8, but not CD4, retained cytotoxic activity.

Thus, the cytotoxic effector cells derived from HCMV seropositive volunteer donors by re-stimulation in vitro with ALVAC recombinants expressing HCMV IE1 (vCP256) or HCMV pp65 (vCP260) were antigen specific, MHC-restricted, and expressed CD3 and CD8. These characteristics are consistent with those of classical cytotoxic T lymphocytes (CTLs).

These results show that ALVAC recombinants expressing HCNV proteins can serve as vaccines for the purpose of eliciting human cytotoxic T lymphocytes capable of mediating the destruction of HCMV-infected human cells. Furthermore, these data also show that these recombinant viruses can serve as reagents for the ex vivo stimulation and expansion of cytotoxic T lymphocyte clones for the purpose of immunotherapeutic applications (Riddell et al., 1992).

As discussed earlier, HCMV-gB can serve to elicit protective immunity in humans since 1) HCMV neutralizing antibody titer is reduced significantly when gB specific antibody is absorbed from human sera (Gönczöl et al., 1991; Marshall et al., 1992) and 2) there is evidence for the activation of helper T cells by the gB protein in seropositive individuals (Liu et al., 1991). Gönczöl et al., (1990) reported the immunoaffinity purified gB was immunogenic in human volunteers. In this study a single injection of the purified gB was able to induce high titers of HCMV neutralizing antibodies and lymphocyte proliferation in naturally seropositive individuals. In seronegative individuals three injections of the gB preparation induced transient HCMV neutralizing antibodies, a fourth injection induced a rapid reappearance and increase in titer of HCMV neutralizing antibodies.

These studies show the use of purified gB as a subunit vaccine. Additionally purified gB can also be used in prime/boost protocols in combination with NYVAC or ALVAC-gB recombinants. Recent studies have indicated that a prime/boost protocol, whereby immunization with a poxvirus recombinant expressing a foreign gene product is followed by a boost with a purified form of that gene product, elicits an enhanced immune response relative to the response elicited with either product alone. For example, humans immunized with a vaccinia recombinant expressing the HIV-1 envelope glycoprotein and boosted with purified HIV-1 envelope glycoprotein from a baculovirus recombinant exhibit higher HIV-1 neutralizing antibody titers than individuals immunized with just the vaccinia recombinant or purified envelope glycoprotein alone (Graham et al., 1993; Cooney et al., 1993). Humans immunized with two injections of ALVAC-HIV (vCP125) failed to develop HIV specific antibodies. Boosting with purified rgp160 from a vaccinia virus recombinant resulted in detectable HIV-1 neutralizing antibodies. Furthermore, specific lymphocyte T cell proliferation to rgp160 was clearly increased by the boost with rgp160. Envelope specific cytotoxic lymphocyte activity was also detected with this vaccination regimen (Pialoux et al., 1995). Macaques immunized with a vaccinia recombinant expressing the simian immunodeficiency virus (SIV) envelope glycoprotein and boosted with SIV envelope glycoprotein from a baculovirus recombinant are protected against a SIV challenge (Hu et al., 1991; 1992).

Example 3.35 Purification of HCMV Glycoprotein B

This Example involves purification of CMV glycoprotein B produced by a vaccinia recombinant, and the testing of its immunogenicity in laboratory animals in combination with ALVAC-CMV gB (vCP139).

COPAK recombinants vP1126, vP1128, and vP1145, each expressing a different form of gB, elicit CMV neutralizing antibodies in mice (Table 8) and therefore express gB in an immunogenic form. To select a virus and cell system, and an immunological reagent for CMV gB purification, gB expression by the three COPAK recombinants was compared by an immunoprecipitation assay, utilizing 5 different gB-specific monoclonal antibodies. Based on the assay results, a scheme was developed to purify gB from the medium of vP1145-infected VERO cells.

Immunoaffinity column bed material was prepared by crosslinking CMV gB-specific monoclonal antibody (mAb) CH380 to Protein A-agarose. This material was used to purify gB in a one-step procedure. Batches of gB were produced and evaluated for purity, as described in section III.

Immunoprecivitation Assay. Vero and HeLa cell monolayers in 60 mm dishes were infected with vP1126, vP1128, vP1145, or vP993 (described below) at an moi of 5 pfu/cell in serum-free medium. Medium and cells were harvested separately at 24 hours post infection. Immunoprecipitation (IP) assays were performed (Taylor et al., 1990) using the reagents described below, with rat anti-mouse IgG as a bridge to protein A for the monoclonals.

Virus

vP1126: COPAK-CMV gB (entire). Full length wild type gB vP1128: COPAK-CMV gB (TM⁻). Lacks transmembrane region vP1145: COPAK-CMV gB (TM⁻, Cl⁻ lacks transmembrane region and has an altered cleavage site. vP993: COPAK control

Reagents

Guinea pig anti-CMV gB: Obtained from Eva Gönczöl (Wistar Institute) Monoclonal CH380: Obtained from PMs&v (Pereria and Hoffman, 1986) Monoclonal 13-127 Advanced Biotechnologies, Inc. Monoclonal 13-128 Advanced Biotechnologies, Inc., neutralizing, conformationally dependent Monoclonal HCMV-34 Cogent Diagnostics, neutralizing Monoclonal HCMV-37 Cogent Diagnostics, neutralizing Rabbit anti-p25 (Vaccinia E3L) (obtained from Bert Jacobs, U. Arizona)

Preparation of immunoaffinity chromatography bed material. One ml of immunoaffinity column bed material consisting of approximately 2.4 mg of mAb CH380 coupled to Protein A-agarose with the crosslinking agent dimethylpimelimidate was provided by Stephen Cockle, Connaught Laboratories, Limited (Willowdale, Ontario, Canada). mAb CH380 (Pereria and Hoffman, 1986) was used previously to purify CMV gB from a CMV viral envelope preparation (Gönczöl et.al., 1990). The material from S. Cockle was used in preliminary experiments to further determine its utility in gB purification. To scale up gB production, additional bed material was prepared by the same method used by S. Cockle, as described below.

Preparation of monoclonal ch380. Four vials of lyophilized monoclonal CH380 (lot S1705, obtained from PMsv) were reconstituted in PBS (137 mM NaCl, 2.7 mM KCl, 1.5 mM KH₂PO₄, 8.1 mM Na₂HPO₄, pH 7.4)(1 ml each) and dialyzed overnight versus PBS (final volume 3.5 ml). Protein concentration was determined to be 4.9 mg/ml by bicinchoninic acid assay (BCA assay, reagents obtained from Pierce, Rockford, Ill.). This preparation was then diluted in an equal volume of MAPS binding buffer (Bio-Rad cat# 153-6161; 31.4% w/v in milli-Q water, adjusted to pH 9, and filtered through a 22 mm membrane). To remove particulate material, the antibody preparation in MAPS buffer was centrifuged at 16,000×g for 30 min, and the protein concentration of the supernate was calculated from the absorbance at 280 nm, using 1.44 as the absorbance coefficient for IgG.

Preparation of protein a-agarose beads. Three ml of protein A-agarose beads (Bio-Rad cat# 153-6153) were washed 4 times with 2 volumes of MAPS binding buffer by gentle mixing in a closed tube and centrifugation for 5 min at 1000×g (1400 rpm in Beckman GPKR centrifuge, GH 3.7 rotor). The supernate was discarded after the last wash.

Binding of monoclonal antibody to the beads. All of the mAb antibody from step 1 was added to the washed beads from step 2 and the mixture was rotated in a closed tube at 4° C. The amount of mAb bound to the beads was determined at 6-12 hour intervals by pelleting the beads (1000 g/5 min) and determining concentration of IgG in the supernatant by reading OD at 280 nm, as described above. Approximately 48 hour of incubation at 4° C. were required to reach 90% depletion of IgG from the supernate.

Covalent crosslinking of monoclonal antibody to the beads. After binding was 90% complete, the beads were washed 4 times with 6 ml (2 volumes) of 50 mM borate, 3M NaCl, pH9. The beads were then resuspended in 30 ml (10 volumes) of 200 mM borate, 3M NaCl, pH9, and the pH adjusted to 9±0.1. A sample of beads (100 μl) was removed for later evaluation of cross-linking. Cross linking reagent dimethylpimelimidate (DMP) was prepared immediately before use at a concentration of 500 mM in 200 mM borate, 3M NaCl, pH9. DMP was added to the beads to produce a final concentration of 20 mM, and the beads were mixed in a closed tube, end-over-end, for 30 min at room temperature. Another sample of beads (100 μl) was removed for evaluation of cross-linking. To quench residual crosslinking reagent, the beads were washed 2 times with 6 ml (2 volumes) of 200 mM ethanolamine, pH8 and then incubated in 30 ml (10 volumes) of 200 mM ethanolamine, pH8 by mixing end-over-end for 2 hours at room temperature. Finally the beads were washed 4 times with 6 ml (2 volumes) of PBS and stored in 6 ml of PBS with 0.01% NaN₃.

To determine the extent of crosslinking, the gel bead samples taken before and after DMP incubation were pelleted, supernates discarded, and the beads mixed with 2×SDS-PAGE sample buffer containing reducing agent. These samples were boiled and electrophoretically separated on a 10% polyacrylamide gel. After staining with Coomassie Blue, IgG heavy and light chains could be detected in the “before” samples, but not in the “after” samples, indicating good efficiency of crosslinking.

Based on protein concentration before and after incubation of the antibody with the beads, the resulting bed material was estimated to contain approximately 5 mg of monoclonal antibody per ml of protein A-agarose beads.

Purification of CMV gB by immunoaffinity column chromatography. Column buffers. PBS (137 mM NaCl, 2.7 mM KCl, 1.5 mM KH₂PO₄, 8.1 mM Na₂HPO₄), pH 7 (batch 1), pH 7.4 (batches 2-5), or pH 6.8 (batches 2-5); 0.1 M glycine, pH 2.5; 1 M tris, pH 8.5.

Columns. Column sizes varied from 0.3 to 4 ml volumes. When a new column was poured, it was stripped with 10 bed volumes (bv) of 0.1 M glycine, pH 2.5, followed by 10-20 bv of PBS, pH 7 or 7.4. At the end of each column run, the column was washed with at least 10 bv of PBS, pH 7. At the beginning of each run, it was washed again with at least 10 bv of PBS, pH 7. The columns were run at room temperature and, when not in use, stored at 4° C. in PBS+0.01% NaN₃.

Preparation of the crude gB sample. Roller bottles (850 cm²) were seeded with Vero cells in MEM+10% FBS. Medium was changed to serum-free MEM 2-12 hours before infection. Cells were infected with vP1145 at an MOI of 5 pfu/cell in a volume of 10 ml/RB of serum-free MEM. Virus was absorbed at 37° C. for 60 min and then 30 ml of serum-free MEM was added to each RB and incubation continued at 37° C. Medium was harvested at 16-24 hours post infection. The medium was clarified by centrifugation at 3000 rpm (Beckman GPKR centrifuge GH 3.7 rotor) for 15 min. The supernatant was recovered and further clarified by centrifugation at 20,000 rpm in a Beckman SW28 rotor for 60 min. The clarified medium was then concentrated (10 to 40-fold) by ultrafiltration with buffer exchange to PBS, pH 7.4, using one or more of the following ultrafiltration devices having 30,000 MWCO: Centricell-60 (Polysciences #19182-6), Centriprep-30 (Amicon #4306), or polysulfone immersible filter units (Polysciences #2250). This material was applied to the column as described below.

Column procedure. The crude gB sample was applied to the column at a flow rate of 0.03-0.09 ml/min, controlled by stopcock or peristaltic pump. After application of the sample, the column was washed at a flow rate of 0.2-0.6 ml/ min with 10 bv PBS, pH7 (batch 1), or 20 bv of PBS, pH7.4 followed by 20 bv of PBS, pH6.8 (batches 2-5). Bound material was eluted with 10 bv of 0.1 M glycine, pH 2.5, collecting 500 μl (Batch 1,3) or 1 ml (batch 2,4,5) fractions into tubes containing 50 μl (Batch 1,3) or 100 μl (batch 2,4,5) of 1.0 M Tris, pH 8.5. One column (#28) was eluted with 0.1N glycine+0.1M Tris, pH7. CMV gB fractions were identified by SDS-PAGE on a 10% gel, under reducing conditions, followed by silver stain (Bio-Rad kit #161-0443).

Treatment of eluted qB. After identification by SDS-PAGE and silver stain the CMV gB fractions were pooled and concentrated in one of 2 ways: 1) Dialysis against 0.1×PBS and 10-fold vacuum concentration (majority of batch 1), or 2) Precipitation with 70% ammonium sulfate and resuspension in PBS. Protein concentration of the gB samples was determined by bicinchoninic acid microplate assay (BCA reagents from Pierce, Rockford, Ill.). Five batches of gB were prepared and frozen in aliquots at −70° C.

Evaluation of purified gB. Slot blot. Slot blot analysis was utilized to measure relative quantities of CMV gB in crude preparations, flow-through fractions, and elution fractions from affinity column purification. Serial two-fold dilutions in PBS were made of each test sample, and these were applied to nitrocellulose paper with the Schleicher and Scheull Manifold II slot blot apparatus. Each test included serially diluted samples of purified gB with a known protein concentration (determined by BCA microplate assay) as a standard. CMV gB was detected with monoclonal CH380 diluted 1:100 followed by ¹²⁵I goat anti-mouse (NEN#NEX159, at 0.1 Ci/ml). Slot blot signals on the autoradiograph were scanned and analyzed by densitometry (PDI, Inc., Huntington Station, N.Y., Quantity One densitometer program). The amount of CMV gB in each test sample was determined by linear regression analysis as compared to a gB standard curve.

Western blot. Test samples were electrophoretically separated on a 10% gel under reducing conditions, and blotted onto nitrocellulose paper (Harlow and Lane, 1988). The blot was probed for the presence of CMVgB, mouse IgG, vaccinia, and Vero cell proteins with the following reagents:

TABLE 7 Detection Methods ANTIGEN PRIMARY ANTIBODY DETECTION CMV gB Monoclonal CH380 ¹²⁵I goat anti-mouse diluted 1:100 (NEN # NEX159), 0.1 μ Ci/ml Mouse ¹²⁵I goat anti-mouse (NEN (See primary antibody) IgG # NEX159, at 0.1 μ Ci/ml Vaccinia Rabbit anti-vP410, ¹²⁵I Protein A (NEN proteins rabbit #W29 week 39, #NEX-146), 0.1 μ Ci/ml 9/13/91, preabsorbed against Vero cells and diluted 1:100 Vero Rabbit anti-Vero cells, ²⁵I Protein A (NEN cell obtained from B. #NEX-146), 0.1 μ Ci/ml proteins Meignier, PMsv, preabsorbed against ALVAC-infected CEF and diluted 1:100

Immunoprecipitation/western blot assay. A combination IP/Western Blot was performed on Batch 1 gB utilizing the panel of monoclonal antibodies. Unlabeled crude and purified gB was subjected to immunoprecipitation followed by SDS-PAGE, the gel was blotted onto nitrocellulose, and gB-specific proteins detected with guinea pig anti-CMV gB (from Eva Gönczöl), diluted 1:1000, and ¹²⁵I Protein A (NEN#NEX-146), 0.1 μCi/ml.

Analysis of the purity of the gB product. Samples from each batch of gB were analyzed by electrophoretic separation on a 10% gel under reducing conditions, followed by staining with Coomassie Blue. The dried gel was scanned and analyzed by densitometry (PDI, Inc., Huntington Station, N.Y., Quantity One densitometer program).

Immunoprecipitation assay comparing expression of CMV gB by three vaccinia COPAK recombinants. To choose a suitable recombinant, cell substrate and antibody for production and immunoaffinity purification of CMV gB, COPAK recombinants expressing 3 different forms of gB were compared by immunoprecipitation assay using guinea pig anti-gB and a panel of monoclonal antibodies. Recombinants vP1126, vP1128, and vP1145 elicit CMV neutralizing antibodies in mice and therefore express gB in an immunogenic form (Table 8). All of the CMV gB antibodies tested produced similar IP results. A representative assay, with guinea pig serum using both medium and cell fractions from HeLa and Vero cell infections, is shown in FIGS. 48A to D. As expected, CMV gB specific material was precipitated from both the cell and medium fractions of vP1128 and vP1145 infected cells, but in only the cell fraction with vP1126 infected cells. The apparent molecular weights of the gB specific bands correspond to previously published results (Britt and Auger, 1986; Britt and Vugler, 1989; Reis et.al., 1993). The cell fractions of all three CMV gB recombinants contained a major band of apparent molecular weight 130-140 kDa, consistent with the apparent molecular weight of the glycosylated uncleaved gB precursor. Less intense protein species with apparent MW of 110 kDa and 55 kDa were observed in the cell fractions and are consistent with the proteolytically processed mature protein species. The N-terminal product was previously reported to be 90-110 kDa and the C-terminal product 55-58 kDa (Britt and Auger, 1986). In HeLa cells a protein species with an apparent higher molecular mass (approximately 150 kDa) was also present (e.g., FIG. 48D, lane 4). This species probably also represents an uncleaved precursor form that is more highly glcosylated. In the medium fractions three gB bands were precipitated from vP1128 and vP1145 infected cells, representing the uncleaved precursor, and N-terminal and C-terminal processed polypeptides. By densitometric analysis, there was more gB-specific material precipitated from the medium fractions of Vero cells compared to HeLa, with recombinant vP1145 producing more gB-specific material than vP1128. This difference may be explained by the observation that more vaccinia E3L was precipitated from the cell fraction of vP1145 than the vP1128 cell fraction, indicating an overall higher level of vaccinia expression in this sample (FIGS. 49A and B). With vP1145, there was more gB specific material precipitated from the medium fraction than from the cell fraction in both HeLa and Vero cells (compare FIGS. 48A,B vs. C,D).

The three different sizes of gB precipitated from the medium of HeLa infected cells appear to have higher molecular weights than the three species produced in Vero cells (compare FIG. 48A vs. 48B). These differences may be due to different levels of glycosylation in HeLa cells compared to Vero, but this hypothesis was not examined further. To determine if the higher molecular weight gB-specific proteins would also be produced by another human cell line, MRC-5, a western blot assay was performed comparing the gB proteins in the medium of vP1145 infected HeLa, MRC-5, and Vero cells using monoclonal CH380 (FIG. 50). The result shows that the two gB bands detectable in this assay, gB precursor (approx. 140 kDa) and C terminal processing fragment (55-58 kDa), had apparently higher molecular weights in HeLa and MRC-5 than in VERO cells. The N-terminal processing fragment is not detectable by western blot using either monoclonal CH380 or the guinea pig anti-CMV gB serum.

MAb CH380 was chosen for use in immunoaffinity purification of gB, since a large quantity was readily available and no apparent differences were seen in the gB-specific proteins detected by the five different monoclonals in the IP assay (FIG. 51). Based on the IP analysis and the considerations that purification of secreted gB from the medium of infected cells eliminates the need to solubilize gB from cell membranes and purify it from cellular proteins, purification of CMV gB was initiated using the medium fraction of vPl145-infected Vero cells. Infection was done in serum-free medium, further reducing contaminating proteins in the crude material.

Purification of CMV gB. Fifteen separate immunoaffinity chromatography column runs, yielding a total of 3.1 mg of gB, are summarized in Table 9. Some of the material was used for further assays and the remainder was pooled in 5 separate batches of purified product, totaling 2.6 mg (Table 10). Column runs 7, 8, 10, and 11 were sequential runs in the same column. The bed material from columns 19A, 19B, 19C, 21A, 21B, and 21C were pooled to make the column used for runs 28, 29, and 32, from which the largest amount of gB was obtained. Table 9 lists the Crude gB material applied to each column in terms of the number of vP1145-infected Vero roller bottles (b 1×10 ⁸ cells per RB) from which the crude material was derived, and amount of total protein and gB-specific protein in the crude. Based on analysis of 8 samples, the total protein content of the crude preparations ranged from 1.2 to 3.7 mg/RB with a mean value of 2.4 mg/RB (24 μg per 10⁶ cells). Utilizing a slot blot assay with purified gB as standard, the amount of gB present in the crude material was measured for 7 of the preparations: values ranged from 50 to 350 μg/RB with a mean of 153 μg/RB (1.5 μg/10⁶ cells). Together these calculations indicate that the protein in the crude preparations consisted of approximately 6% gB. CMV gB yields ranged from 8 to 29 μg/RB with a mean of 20 μg/RB (0.2 μg/10⁶ cells) (Table 9). Approximately fifty roller bottles (1×10⁹ cells) were required to produce 1 mg of CMV gB.

The capacity of the immunoabsorbent gel for gB was not fully evaluated. The 4 ml bed material used for column runs 28, 29, and 32, was initially divided into 0.6 ml mini-columns (column runs 19A, 19B, 19C, 21A, 21B, and 21C) and varying amounts of crude gB were applied to each column to determine where saturation of binding would occur. Unfortunately, the quantity of gB in the crude material applied to the columns was overestimated, and saturation was not demonstrated. The highest binding result (from column 19C) was used as an estimate of column capacity (300 μg/ml bed material). The amount of gB eluted from the mini-columns represented 8 to 25% of the gB protein applied to the columns (Table 9). Therefore, if the capacity of the 4 ml column is at least 1.2 mg and 25% of the gB applied is recovered, it was estimated that 4.9 mg of crude gB (from approximately 33 RB) must be applied to the column to obtain 1.2 mg of purified gB. The result from column 28 is close to this estimate: material from 36 roller bottles was applied to the column #28, and 1 mg of gB was eluted.

The gB applied to the columns but not eluted as purified material has not been quantitatively accounted for. Since only 8-25% of the gB applied to the column was recovered as purified gB, the remainder of the gB must be present in flow-through fractions, wash fractions, eluted fractions not pooled with the product, or bound to the column. CMV gB could be detected by western blot in the flow-through fractions (e.g., FIG. 52, lane 6). However, when the amount of gB in the flow-through fractions was estimated by slot blot analysis, it did not account for more than 20% of the applied gB. The wash fractions have not been evaluated. The pooled fractions chosen for the final gB product were peak fractions only and therefore trace amounts of gB in adjacent fractions could account for some of the missing gB. For example, FIG. 53 shows sequential fractions eluted from column 8. Fractions 8.17-8.21 were pooled for the gB product, but trace amounts remained in fractions 8.16 and 8.22. Evidence exists also for the retention of gB in the immunoabsorbent gel. Gel material, taken from columns 11 and 19C after elution and washes, contains gB specific material detectable by western blot (FIG. 52, lanes 2 and 3). The amount of gB remaining on the column has not been quantitatively evaluated.

Reapplication of flow-through material to the column was attempted when flow-through material from column run #7 was applied to column #10 (Table 9). The amount of gB eluted from column 10 (4.5 μg) was only 4% of that obtained from column 7 (110 μg). It was not possible to evaluate this result since the capacity of the bed material for gB, and the amounts of gB applied to the column and present in the flow-through fractions were not known. Because of the poor yield, this approach was not used again.

Evaluation of purified gB. After pooling gB-containing eluted fractions, evaluation of purified gB consisted of 1) determination of total protein concentration, 2) SDS-PAGE analysis to identify gB specific and non-specific bands, and 3) confirmation of these bands with immunological reagents. Additionally, the purified gB was analyzed for degree of purity by densitometer scan, and for native conformation by ability to bind to a panel of CMV monoclonal antibodies.

Fractions containing CMV gB eluted from each column were analyzed initially by SDS-PAGE and silver staining, and gB fractions were identified and pooled for each run. A typical elution profile is shown in FIG. 53. A portion of the eluted gB was used for analysis, and the remainder of the material was combined into 5 separate batches (Table 10). Each batch was analyzed by SDS-PAGE on a 10% gel under reducing conditions and stained with Coomassie Blue (FIG. 54). The stained gel was scanned on a densitometer and the molecular weight and relative quantity of each band was calculated: a typical scan is shown in FIGS. 55, 55A and analysis of the 5 batches is summarized in Table 11. By SDS-PAGE analysis batches 1-5 appear very similar (FIG. 54). The two major bands, having apparent molecular weights 120-130 and 51-59 kDa, represent the precursor gB protein and the C-terminal processing fragment. The wide diffuse appearance of these bands is probably due to variable glycosylation of this normally heavily glycosylated protein. The identity of these bands as gB-specific is supported by results from western blot analysis with monoclonal CH380 (FIG. 56B). The bands of apparent molecular weight 77-100 kDa, which appear as doublets in batches 2-5 (FIG. 54), are the correct size for the gB N-terminal processing fragment, identified in the medium of vP1145-infected cells by IP analysis (FIGS. 48A and B). These bands could not be verified as gB-specific by either western blot analysis (FIG. 56B), or a combination immunoprecipitation-western blot assay (FIGS. 57A and B), but the possibility should not be ruled out since neither the guinea pig anti-gB serum nor monoclonal CH380 are able to detect N-terminal processing fragments by western blot. A contaminating protein of approximately 39-45 kDa is present in each batch at a level of 6-15% of total protein (FIG. 54 and Table 11). Two more possible gB protein bands, one of greater than 200 kDa and the other 30-35 kDa are present in every batch (FIGS. 54, 55, and 55A; Table 11). Evidence that the large (˜200 kDa) protein is gB is derived from western blot analysis with monoclonal CH380 which detects two proteins with molecular weights greater than 200 kDa (FIG. 56B, lanes 2 & 3). It is possible that the protein of approximately 30-35 kDa is also gB-specific (FIG. 54). In the IP analysis of medium of vP1145-infected cells, a protein of approximately 35 kDa was detected by 3 monoclonals (13-128, HCMV 34, and HCMV 37)(FIG. 51) and by the guinea pig serum (FIGS. 48A and B). A protein of this size was described by Reis et al. (1993) as a degradation product of gB.

Assuming that contaminating proteins in the gB preparation would be derived from the cell substrate, the virus vector or the immunoabsorbent bed material, the preparation was probed for the presence of mouse IgG, Vero cell proteins, and vaccinia proteins. Proteins derived from Vero cells or mouse IgG could not be detected by western blot analysis (FIGS. 56A and 58A). However, contaminating vaccinia-specific proteins with molecular weights of approximately 35 and 20 kDa were detected in trace amounts (FIG. 58B, lane 5).

To determine if the eluted gB retained its native conformation, a combination immunoprecipitation/western blot assay was performed with a panel of monoclonals which included 3 neutralizing and one conformationally dependent antibody. Each monoclonal antibody precipitated the precursor and C-terminal fragment from purified gB (FIG. 57), suggesting that the gB eluted from the immunoaffinity column retained its native conformation.

In summary, the analysis of eluted gB in batches 1-5 demonstrates that the product contains at least two known gB-specific proteins, the precursor gB and C-terminal fragment, which together account for approximately 50% of the protein content (FIG. 54 and Table 11). Three other protein species, which account for 20-25% of total protein content (Table 11), could also be gB-specific although direct evidence has not been provided.

Furthermore, this Example provides both general and specific techniques for isolation and/or purification of HCMV epitope(s) of interest, which can be applied analogously to whole cell preparations infected with HCMV.

Immunogenicity of purified gB. The five CMV gB batches were pooled and the final concentration determined. Several amounts of purified gB were adjuvanted with either alum or QS21 and used to inoculate mice. Serum from the mice was evaluated for the presence of HCMV neutralizing antibody. Table 12 demonstrates that all of the amounts of purified gB tested with both adjuvants were able to elicit HCMV neutralizing antibody.

Purified gB was used in a prime/boost protocol in combination with ALVAC-gB (vCP139) in mice. Table 13 demonstrates that mice receiving ALVAC gB (vCP139) on day 0 and boosted on Day 29 with purified gB adjuvanted with QS21 or Alum developed higher levels of HCMV neutralizing antibody than mice receiving a second dose of ALVAC-gB (vCP1319).

TABLE 8 Induction of HCMV Neutralizing Antibody in Mice Days After Immunization Immunogen¹ 30 48 135 vP1126 16² 8 256 vP1128 16  8 106 vP1145 16  8 106 ¹Mice were immunized with 1 × 10⁸ PFU of recombinant viruses (ip.) on day 0 and day 49. ²HCMV Neutralizing titer

TABLE 9 SUMMARY OF IMMUNOAFFINITY PURIFICATION COLUMNS CRUDE MA- TERIAL APPLIED # VERO TO COLUMN COLUMN ROLLER gB-specific gB YIELD RUN BOTTLES^(a) COLUMN SIZE Total Protein^(b) protein^(c) (% of applied) 7 4 1 ml 13.3 mg nd^(d) 110 μg^(b) 8 6 1 ml 14.4 mg 2.2 mg 84 μg^(b) 10 Col 7 1 ml nd nd 4.8 μg^(b) flow thru 11 4 1 ml nd nd 100 μg^(b) 13 1 0.3 ml nd nd 12 μg^(d) 19A 1 0.6 ml 2.9 mg 240 μg 41 μg^(c) (17%) 19B 2 0.6 ml 5.8 mg 480 μg 93 μg^(c)(19%) 19C 3 0.6 ml 8.7 mg 720 μg 185 μg^(c) (25%) 21A 3 0.6 ml 5.7 mg 300 μg 29 μg^(c)(8%) 21B 5 0.6 ml 9.5 mg 500 μg 120 μg^(c) (13%) 21C 7 0.6 ml 13.3 mg 700 μg 150 μg^(c) (19%) 23 3 6 ml 5.7 mg 300 μg 25 μg^(c) (8%) 28 36 4 ml 64.8 mg nd 1000 μg^(b) 29 24 4 ml 30 mg nd 480 μg^(b) 32 24 4 ml nd nd 700 μg^(b) ^(a)Cell density: 1 × 10⁸ cells per roller bottle ^(b)Protein concentration determined by Pierce BCA assay ^(c)Estimated by slot blot analysis, using purified gB as standard ^(d)Not determined

TABLE 10 CMV gB BATCHES TOTAL COLUMN BATCH # gB VOLUME CONCENTRATION RUN 1 0.16 mg 0.55 ml 0.29 mg/ml 7 8 10 11 13 2 1.0 mg 1.0 ml 1.0 mg/ml 28 3 0.26 mg 0.5 ml 0.52 mg/ml 21A 21B 21C 23 4 0.48 mg 0.5 ml 0.96 mg/ml 29 5 0.7 mg 0.5 ml 1.4 mg/ml 32

TABLE 11 DENSITOMETRY ANALYSIS OF 5 BATCHES OF CMV gB PROTEIN APPARENT MOLECULAR WEIGHT (kDa)^(a) RELATIVE QUANTITY (%)^(b) BAND B1 B2 B3 B4 B5 B1 B2 B3 B4 B5 >200 kDa 222 208 221 225 217 10.6 6.7 7.5 8.3 7.4 (gB?) 192 8 Precursor gB 128 120 124 128 134 39 30 36.1 30 27.4 N fragment 83 94 99 101 100 9.6 3.6 3.2 4.5 3.5 (?) 77 84 88 89 9.7 6.3 6.6 6.3 6.3 C fragment 55 51 55.4 56.4 59 21 15.6 13.7 22.6 21 Unknown 42 39 42 44 45 6.1 12 15.4 14.3 15.8 contaminant gB 32 30 35 35 37 4.3 9.7 11.3 8.6 10 degradation product (?) ^(a)Calculated from densitometer scan using molecular weight markers as standards (refer to FIG. 55, 55A) ^(b)The density of each band is calculated from a 2 dimensional scan line through the band: the average pixel OD across the sample width is integrated under the curve to the baseline to obtain density (OD × cm). Relative quantity is the percentage of the total density of all bands in the lane. (refer to FIG. 55, 55A).

TABLE 12 HCMV Neutralizing Antibodies Elicited by purified gB protein in CBA Mice¹ NT² NT² NT² NT² Mouse dose³ Adjuvant³ 4w 6w 8w 9w 201 2.5 Alum 32 256 256 256 203 8 64 128 128 204 8 12 16 16 206 5.0 Alum 48 512 192 192 207 12 192 512 512 208 16 192 192 192 209 16 128 256 256 210 8 128 256 256 211 10.0 Alum 32 256 213 32 96 256 256 214 32 256 256 216 20.0 Alum 64 128 128 128 217 64 256 256 256 218 32 128 512 256 219 16 128 256 256 220 32 192 512 256 222 2.5 QS21 8 192 512 223 32 >4096 >4096 2048 224 16 1536 225 64 1024 1024 1024 226 5.0 QS21 64 >4096 1024 1024 227 96 >4096 228 64 >4096 >4096 >4096 229 64 >256 >4096 230 32 >4096 1536 2048 231 10.0 QS21 64 2048 2048 >4096 232 96 1536 2048 233 96 >4096 234 64 2048 2048 1024 236 20.0 QS21 128 3072 239 96 >4096 >4096 >4096 ¹Mice were inoculated S.C. at weeks 0 and 4. ²Sera were obtained at 4, 6, 8 or 9 weeks after priming. ³μg gB in either 15 μg QS21 or 25 μl Alum were used for each inoculation.

TABLE 13 Summary Of Prime-Boost Experiment antigen antigen NT adj. NT adj. NT NT Mice Day 0 Day 29 Day 42 Day 56 381 4 ALV 32 gB + Alu 384 768 382 <4 ALV 8 gB + Alu 192 192 383 4 ALV 4 gB + Alu 192 256 384 <4 ALV 48 gB + Alu 512 512 385 4 ALV 16 gB + Alu 256 ND 397 4 ALV 8 gB + Alu 128 192 G.m. 4 13.5 248 326 392 <4 ALV <4 gB + QS 128 128 393 <4 ALV 4 gB + QS >1024 >1024 394 <4 ALV 8 gB + QS >1024 >1024 395 <4 ALV 16 gB + QS 512 384 396 <4 ALV 4 gB + QS 256 384 398 4 ALV 8 gB + QS >1024 >1024 G.m. 4 6.3 >512 >522 373 4 ALV 16 ALV 128 96 376 4 ALV 4 ALV 8 12 378 8 ALV 4 ALV 8 4 379 4 ALV 8 ALV 128 128 380 4 ALV 16 ALV 64 64 399 4 ALV 4 ALV 96 192 400 <4 ALV 4 ALV 64 128 G.m. 4 6.5 45.6 51.2 5 × 10⁵ TCD₅₀ of ALVAC-gB (vCP139), 5 ug gB + Alu, 1 ug gB + QS21 were given, s.c. G.m. = geometric mean

The results presented here demonstrate the ability of the NYVAC and ALVAC-HCNV recombinants and products therefrom to be employed in the compositions and utilities aforementioned, for instance, immunological, antigenic or vaccine compositions, or for use in preparing antigens or antibodies for assays, kits or tests, and, for example, as suitable for uses in vaccine or immunization strategies capable of preventing vascular disease such as restenosis and/or atherosclerosis arising from infection by HCMV; and, that the DNA of the recombinants is useful for probes or for preparing PCR primers for diagnosis of restenosis and/or atherosclerosis or whether a patient is prone thereto or not prone thereto due to HCMV status.

Example 3.36 Expression of CMV Genes in NYVAC-CMV6 (vP1302B) and NYVAC-CMV5

Immunoprecipitation with monoclonal antibodies specific for gB, gH, pp65, pp150 and IE1-exon4 demonstrated the correct expression of these five genes by NYVAC-CMV6. FACScan analysis (Becton-Dickinson) demonstrated surface expression of gH in vP1302B infected cells but not in cells infected with its parent (vP1251) indicating that a functional gL gene product is expressed in vP1302B.

Immunoprecipitation with monoclonal antibodies specific for gB, gH, pp65 and pp150 demonstrated the correct expression of these four genes by NYVAC-CMV5 (vP1312). FACScan analysis demonstrated surface expression of gH in vP1312 infected cells but not in cells infected with its parent (vP1262) indicating that a functional gL gene product is expressed in vP1312.

Example 3.37 Developing an ALVAC Donor Plasmid Containing the HCMV pp65 and pp150 Genes

Plasmid CMV65C6.2 was linearized with EcoRI, filled in with klenow and treated with alkaline phosphatase generating a 6.3 kb fragment. Plasmid 150.1 was digested with NheI, filled in with klenow and a 3.2 kb fragment (42K-pp150) isolated. Ligation of these two fragments yielded plasmid 150.8R1 in which transcription of pp65 and pp150 are in the same direction and pp150 is reversed from plasmid 150.8 in Example 3.29. The DNA sequence of CMVpp65 and CMVpp150 plus additional flanking sequences in plasmid 150.8R1 are shown in FIGS. 59A-C (SEQ ID NO:38).

Example 3.38 Construction of ALVAC-CMV4 (gB, gH, pp65, pp150)

Plasmid 150.8R1 was transfected into vCP233 infected CEF cells to generate ALVAC-CMV4 (vP1360).

Example 3.39 Expression of CMV Genes in ALVAC-CMV4

Immunoprecipitation with monoclonal antibodies specific for gB, gH, pp65 and pp150 demonstrated the correct expression of all four genes by ALVAC-CMV4 (vP1360).

Example 3.40 Developing ALVAC Donor Plasmids Containing HCMV gL OR gL Plus IE1-exon4

FIGS. 60A and B (SEQ ID NO:39) is the sequence of a 5.8 kd segment of canarypox DNA contained in plasmid pCPtk. The canarypox thymidine kinase gene (tk) is encoded within this segment initiating at nucleotide 4412 and terminating at nucleotide 4951. A tk (C7) insertion vector containing 2085 bp upstream of C7, polylinker containing SmaI, NruI, EcoRI, XhoI and StuI sites, and 812 bp downstream of C7 was derived in the following manner. A 3450 bp PstI/NsiI fragment from pCPtk was cloned into the blunt ended Asp718/XbaI sites of PBS-SK+ generating plasmid pEU1. To delete the tk ORF and replace it with a polylinker, two PCR fragments were amplified from pCPtk using oligonucleotides RG578 (SEQ ID NO:153) (5′-GTACATAAGCTTTTTGCATG-3′) plus RG581 (SEQ ID NO:154) (5′-TATGAATTCCTCGAGGGATCCAGGCCTTTTTTATTGACTAGTTAATCAGTCTAATATACGTACTA AATAC-3′) and RG579 (SEQ ID NO:155) (5′-CTAATTTCGAATGTCCGACG-3′) plus RG580 (SEQ ID NO:156) (5′-TTAGAATTCTCGCGACCCGGGTTTTTATAGCTAATTAGTACTTATTACAAATACTATAATATTTA G-3′). These fragments were purified, digested with HindIII/EcoRI or BstBI/EcoRI and ligated to pEU1 cut with HindIII/BstBI resulting in plasmid pC7.

The polylinker region in pC7 was modified in the following manner. pC7 was digested with EcoRI and StuI, purified and ligated to annealed oligonucleotides SDSYN154 (SEQ ID NO:157) (5′-AATTCGTCGACGGATCCCTCGAGGGTACCGCATGC-3′) and SDSYN155 (SEQ ID NO:158) (5′-GCATGCGGTACCCTCGAGGGATCCGTCGACG-3′) generating plasmid pC7⁺.

Plasmid pC7⁺ was digested with BamHI and treated with alkaline phosphatase. Plasmid I4LH6CgL was digested with BamHI and BglII and a 968 bp fragment (containing the H6 promoted gL gene ) isolated. Ligation of these two fragments generated plasmid C7gL in which transcription of gL is in the same direction as the deleted tk gene. The DNA sequence of HCMV gL plus additional flanking sequences in plasmid C7 gL is shown in FIGS. 61A and B.

Plasmid C7 gL was digested with BamHI and PspAI and treated with alkaline phosphatase. Plasmid I4LH6IEEX4 was digested with BamHI and PspAI and a 1363 bp fragment (containing the H6 promoted IE1-exon4 gene) isolated. Ligation of these two fragments yielded plasmid C7gLIES2. The DNA sequence of HCMV gL and IE1-exon4 plus additional flanking sequences in plasmid C7gLIES2 is shown in FIGS. 62A and B.

Example 3.41 Construction of ALVAC-CMV6 (gB, gH, gL, pp65, pp150, IE1-exon4 and ALVAC-CMV5 (gB, gH, gL, pp65, pp150)

Plasmid C7gLIES2 is transfected into vP1360 infected cells to generate ALVAC-CMV6 (gB, gH, gL, pp65, pp150 , IE1-exon4).

Plasmid C7 gL is transfected into vP1360 infected cells to generate ALVAC-CMV5 (gB, gH, gL, pp65, pp150).

Example 3.42 Cloning of HCMV gL and A gH Lacking its Transmembrane Region and Cyoplasmic Tail in NYVAC Donor Plasmid RSD553

The sequence of HCMV gH lacking its transmembrane region and cytoplasmic tail is presented in FIG. 63 (SEQ ID NO:41). Plasmid SPgH1 was used in PCR with oligonucleotides SPgHS1 (SEQ ID NO:159) (5′-CCGAAGCTTCTCGAGATAAAAATCAACGACTGTCGGTAGCGTCCACGACGAC-3′) and SPgH8 (SEQ ID NO:160) (5′-TCCACTCCATGCTAGT-3′) to generate a 756 bp fragment. This fragment was digested with NsiI and HindIII and a 275 bp fragment isolated. Plasmid SPgH6 was digested with NsiI and HindIII and a 4779 bp fragment isolated. Ligation of these two fragments yielded plasmid SPgH7 which contains the 42K promoted gH gene lacking its transmembrane region and cytoplasmic tail.

NYVAC insertion plasmid pSD553 was digested with BamHI and treated with alkaline phosphatase. Plasmid I4LH6CgL was digested with BamHI and BglII and a 970 bp fragment (containing the H6 promoter and gL gene) isolated. Ligation of these two fragments generated plasmid COPAKgL-24.

Plasmid gH7 was digested with XhoI and ScaI and a 2239 bp fragment isolated (containing the 42K promoter and truncated gH gene). Plasmid COPAKgL-24 was digested with XhoI, treated with alkaline phosphatase and ligated to the 2239 bp fragment generating plasmid COPAKHL-15. The DNA sequence of gL and the truncated gH plus additional flanking DNA sequences in plasmid COPAKHL-15 is shown in FIGS. 64A and B (SEQ ID NO:42).

Example 3.43 Constructing a Poxvirus Recombinant Containing gL and gH Lacking Transmembrane Region and Cytoplasmic Tail

Plasmid COPAKHL-15 was transfected into NYVAC infected CEF cells to generate the recombinant vP1399.

Example 3.44 Expression of gH by Recombinant VP1399

Immunoprecipitation with a monoclonal antibody specific for gH revealed the expression of a secreted gH protein of approximately 97 kDa by recombinant vP1399.

Example 4 Poxvirus-p53 Epitope of Interest Recombinants

Reference is made to WO 94/16716, incorporated herein by reference, with respect to this Example, especially Examples 15, 32 and 33, and FIGS. 17, 18, 38 and 39 of WO 94/16716. Methods and Materials are as in Example 3.

Example 4.1 NYVAC- and ALVAC-p53 Recombinant Viruses

The nuclear phosphoprotein, p53, is found in normal cells at very low steady state levels. Expression of p53 is tightly regulated throughout the cell cycle and may be involved in controlling cell proliferation. The molecular mechanisms by which p53 exerts its tumor suppressor activity remain unknown, although p53 appears to exist in two conformational states. One form is unique to wildtype p53 and is associated with the ability to block cell cycle progression while the second form is associated with the ability to promote cell proliferation and is common to wildtype and mutant forms (reviewed by Ulrich et al., 1992). p53 is the gene most frequently found to be mutated in a wide variety of human tumors (reviewed by Hollstein et al., 1991).

Probably the most studied cancer associated with p53 mutation is breast cancer. It is known that p53 mutation results in the overexpression of the p53 gene product in primary breast cancer patients (Davidoff et al., 1991). The basis for p53 overexpression was found to result from a post-transcriptional mechanism, since p53-specific mRNA levels were similar in tumors with high and low level protein expression. Further, the p53 mRNA from overexpressing tumors were found to contain missense mutations in highly conserved regions of the gene. These mutations were subsequently found to give rise to more stable p53 protein forms which form complexes with heat shock protein 70 (HSP-70). Since HSP-70 proteins have been implicated in antigen processing, not only may the humoral response to p53 observed in a subset of breast cancer patients have resulted from unique processing/presentation modes for complexes, such an association may also elicit cellular anti-p53 protein responses (Davidoff et al., 1992). Such anti-p53 cellular immune responses are responses more germane to the immunotherapy of such cancers.

Generation of Poxvirus-based Recombinant Viruses Expressing Wildtype and Mutant Forms of the Human p53 Gene Product

Three plasmids, p53wtXbaISP6/T3, p53-217XbaI, and p53-238XbaI containing wildtype human p53 gene sequences, and two mutant forms of p53, respectively, were obtained from Dr. Jeffrey Marks (Duke University). The p53-217XbaI contains a p53 gene encoding a p53 product lacking codon 217 while p53-238XbaI encodes a p53 gene product with an cysteine to arginine substitution at amino acid 238. The sequence of the wildtype p53 cDNA and the deduced amino acid sequence was described previously (Lamb and Crawford, 1986).

All three p53 genes were individually juxtaposed 3′ to the modified vaccinia virus H6 promoter described by Perkus et al., 1989. These manipulations were performed in the following manner. A 227 bp PCR-derived fragment was generated using oligonucleotides MM002 (SEQ ID NO:161) (5′-GATCTGACTGCGGCTCCTCCATTACGATACAAACTTAACGG-3′) and RW425 (SEQ ID NO:162) (5′-GTGGGTAAGGGAATTCGGATCCCCGGGTTAATTAATTAGTGATAC-3′) and plasmid pRW825 as template. PCR using these oligonucleotides amplifies the vaccinia H6 promoter sequences from pRW825 such that the 3′ end of the promoter is precisely linked to the 5′-most region of the p53 coding sequence. Plasmid pRW825 contains the vaccinia virus H6 promoter (Perkus et al., 1989) linked to a nonpertinent gene.

PCR was also used to generate a 480 bp and 250 bp fragment from p53wtXbaISP6/T3. The 480 bp fragment was derived with oligonucleotides MM003 (SEQ ID NO:163) (5′-GTTTGTATCGTAATGGAGGAGCCGCAGTCAGATC-3′) and MM008 (SEQ ID NO:164) (5′-CATTACGATACAAACTTAACGGATATCGCGACGCGTTCACACAGGGCAGGTCTTGGC-3′). This fragment contains the 3′ portion of the vaccinia virus H6 promoter sequences and the 5′ portion of the p53 coding sequences through the SgrAI site. The 250 bp fragment was derived by amplification with oligonucleotides MM005 (SEQ ID NO:165) (5′-TACTACCTCGAGCCCGGGATAAAAAACGCGTTCAGTCTGAGTCAGGCCC-3′) and MM007 (SEQ ID NO:166) (5′-GTGTGAACGCGTCGCGATATCCGTTAAGTTTGTATCGTAATGCAGCTGCGTGGGCGTGAGCGCTTC-3′). This PCR fragment contains the 3′ end of the p53 coding sequences beginning at the StuI restriction site. The 480 bp and 250 bp PCR fragments were generated such that the 5′ end of the MM005/MM007-derived (SEQ ID NO:165/166) fragment overlaps the 3′ end of the MM003/MM008-derived (SEQ ID NO:163/164) fragment.

The 227 bp, 480 bp, and 250 bp PCR-derived fragments were pooled and fused by PCR using oligonucleotides MM006 (SEQ ID NO:167) (5′-ATCATCGGATCCCCCGGGTTCTTTATTCTATAC-3′) and MM005 (SEQ ID NO:165). The 783 bp fused PCR product contains the H6 promoter juxtaposed 5′ to the 5′ portion of the p53 coding sequence (through the SgrAI restriction site) followed by the end of the p53 coding sequence beginning at the StuI site. Following the end of the p53 coding sequence, a T₅NT sequence motif providing early vaccinia transcription termination (Yuen and Moss, 1986) and a unique XhoI site were added. It should be noted that the final H6-p53 PCR fusion product (783 bp) does not contain the p53 coding sequences between the SgrAI and StuI restriction sites.

The 783 bp fusion was digested with BamHI (5′ end) and XhoI (3′ end) and inserted into plasmid pSD550 to yield plasmid pMM105.

Plasmids containing intact p53 gene (wildtype or mutant forms) juxtaposed 3′ to the H6 promoter were generated by first digesting pMM105 with SgrAI and StuI. A 795 bp SgrAI/StuI fragment was isolated from p53wtXbaISP6/T3 and p53-238XbaI, while a 792 bp fragment was isolated from p53-217XbaI. These fragments were individually ligated to the SgrAI/StuI digested pMM105 plasmid to yield pMM106, pMM108, and pMM107, respectively.

Plasmids pMM106, pMM107, and pMM108 were used in standard in vitro recombination experiments (Piccini et al., 1987) with NYVAC (vP866; Tartaglia et al., 1992) as the rescue virus to generate recombinant viruses vP1101, vP1096, and vP1098, respectively. FIG. 77 presents the nucleotide sequence of the wildtype p53 expression cassette and flanking regions within vP1101 (SEQ ID NO:168). The H6 promoter starts at position 145. The p53 start codon is at position 269, and the p53 stop codon is at position 1450. Positions 1 through 144 and positions 1451 through 1512 flank the H6/p53 expression cassette. The sequences within vP1096 and vP1098 are identical except vP1096 contains a 3 base deletion from nucleotide 920 to 922 while vP1101 contains a point mutation at nucleotide 980 (T or C).

Both immunofluorescence and immunoprecipitation assays were performed using a p53-specific monoclonal antibody (pAB1801, Oncogene Science provided by Dr. J. Marks) to demonstrate expression of p53 in vP1101, vP1098 and vP1096 infected Vero cells. These assays were performed as described previously (Taylor et al., 1990). Immunofluorescence assay demonstrated p53-specific fluorescent staining of cells infected with vP1101, vP1096, or vP1098. The p53 antigen was located in both the nucleus and cytoplasm of the infected cells. The nuclear staining, however, was more intense in vP1101 infected cells. These results are similar to those reported by Ronen et al. (1992) using replication-competent vaccinia to express wildtype and mutant forms of p53. No p53-specific fluorescent staining was observed in Vero cells infected with the parental NYVAC virus, vP866.

ALVAC (CPpp) p53 insertion plasmids were engineered by excising the p53 expression cassettes from pMM106, pMM107, and pMM108 by digestion with BamHI and XhoI and inserting them individually into BamHI/XhoI digested NVQC5LSP. The 1320 bp BamHI/XhoI fragment containing the H6-p53 expression cassette from pMM106 and pMM108 was inserted into NVQC5LSP to yield pMM110 and pMM112, respectively, while the 1317 bp BamHI/XhoI fragment derived from pMM107 and inserted into NVQC5LSP yielded pMM111. (NVQC5LSP generated by introducing a NotI site in pVQC5LSP6, generated from pC5LSP, which in turn was generated from pCL5, which in further turn was generated from pC5LAB, which was generated from PHCOS1, which originated from 1535 bp upstream polylinker containing KpnI, SmaI, XbaI, and NotI sites and 404 bp of canarypox DNA, e.g., 31 bp of C5 coding sequence and 373 bp of downstream sequence, and cosmid vector pVK102; see FIG. 65 (SEQ ID NO:43), providing nucleotides 1-1372 of ClaI fragment from pHCOS1 containing C5 region.)

Insertion plasmids pMM110, pMM111, and pMM112 were used in standard in vitro recombination experiments (Piccini et al., 1987) with ALVAC (CPpp) as the rescue virus to yield vCP207, vCP193 and vCP191, respectively. Confirmation of expression of the p53 gene product was accomplished by immunoprecipitation assays performed as described above. FIG. 66 presents the nucleotide sequence of the H6/p53 (wildtype) expression cassette and flanking regions from vCP207 (SEQ ID NO:44). The H6 promoter starts at position 109. The p53 start codon is at position 233, and the p53 stop codon is at position 1414. Positions 1 through 232 and positions 1415 through 1483 flank the H6/p53 expression cassette. The nucleotide sequence is identical to that within vCP193 and vCP191 except vCP193 contains a 3 nucleotide deletion from nucleotide 973 to 975 while vCP191 contains a point mutation at nucleotide 94 to (T to C).

A listing of the NYVAC- and ALVAC- based p53 recombinant viruses is provided in Table 14.

TABLE 14 NYVAC and ALVAC-based p53 recombinant viruses Recombinant Virus Parent Virus Gene Insert vP1101 NYVAC w.t. 53 pP1096 NYVAC p53(−aa 217) pP1098 NYVAC p53 (aa238; C to R) vCP207 ALVAC w.t. 53 vCP193 ALVAC p53 (−aa 217) vCP191 ALVAC p53 (−aa 238; C to R)

Example 4.2 Insertion of Wildtype and Mutant Forms of Murine P53 into ALVAC

The gene for the nuclear phosphoprotein p53 is the gene most frequently found to be mutated in a wide variety of human tumors (reviewed in Hollstein et al., 1991). NYVAC and ALVAC-based p53 recombinant virus are described in Example 4.1.

Insertion of wildtype Murine p53 into ALVAC. Plasmid p11-4 containing murine wild-type p53 was received from Arnold Levine (Princeton University, Princeton, N.J.). The p53 sequence is described in Pennica et al., (1984). The murine wild-type p53 gene was placed under the control of the vaccinia H6 promoter and the p53 3′ non coding end was removed with PCR-derived fragments.

A fragment containing the H6 promoted 5′ end of the p53 gene fused to the 3′ end of the p53 gene was generated by several PCRs as described below.

PCR I: Plasmid pRW825, containing the H6 promoter and a nonpertinent gene, was used as template with oligonucleotides MM080 (SEQ ID NO:169) 5′ATTATTATTGGATCCTTAATTAATTAGTGATACGC 3′ and MM081 (SEQ ID NO:170) 5′CTCCTCCATGGCAGTCATTACGATACAAACTTAAC 3′ producing a 228 bp fragment containing the H6 promoter and the 5′-most base pairs of the murine p53 gene. MM080 anneals to the 5′ end of the H6 promoter and primes toward the 3′ end. MM081 anneals to the 3′ end of the H6 promoter and primes toward the 5′ end.

PCR II: Plasmid p11-4 was used as template with oligonucleotides MM082 (SEQ ID NO:171) 5′CGTTAAGTTTGTATCGTAATGACTGCCATGGAGGAGTC 3′ and MM083 (SEQ ID NO:172) 5′TAGTAGTAGTAGTAGCTTCTGGAGGAAGTAGTTTCC 3′ to generate a 129 bp fragment with the 3′-end of the H6 promoter, the 5′ end of the p53 gene followed by 15 bp which overlaps PCR fragment PCRIII (described below). MM082 contains the 3′ end of the H6 promoter and primes from the 5′ end of the murine p53 gene. MM083 anneals to position 97 (FIG. 67) of the murine p53 gene and primes toward the 5′ end.

PCRIII: Plasmid p11-4 was used as template with oligonucleotides MM084 (SEQ ID NO:173) 5′CAGAAGCTACTACTACTACTACCCACCTGCACAAGCGCC 3′ and MM085 (SEQ ID NO:174) 5′AACTACTGTCCCGGGATAAAAATCAGTCTGAGTCAGGCCCCAC 3′ to generate a 301 bp fragment. The 301 bp PCR-derived fragment contains the 3′ end of the p53 gene, and the 5′ end overlaps the 3′ end of the PCRII product. MM084 (SEQ ID NO:173) primes from position 916 of the murine p53 gene toward the 3′ end. MM085 (SEQ ID NO:174) primes from position 1173 toward the p53 gene 5′ end. The three PCR products were pooled and primed with MM080and MM085. The resultant 588 bp fragment contains a BamHI site followed by the H6 promoted 5′ end of the p53 gene fused to the p53 gene 3′ end followed by a SmaI site; the 5′ end of the p53 gene ends at the XhoI site at position 37, and the 3′ end starts at the SacII site at position 990 (FIG. 67). The 588 bp PCR-derived fragment was digested with BamHI and SmaI generating a 565 bp fragment which was inserted into BamHI/SmaI digested pNC5LSP5 (described below). The resultant plasmid, designated pMM136, was digested with KspI and XhoI to remove a 149 bp fragment, and the 953 bp KspI/XhoI fragment from p11-4 was inserted. The resultant plasmid, pMM148, contains the H6 promoted wild-type murine p53 in the ALVAC C5 insertion locus.

The construction of pNC5LSP5 is as follows. A C5 insertion vector plasmid C5LSP (Example 3.5) was digested with EcoRI, treated with alkaline phosphatase and ligated to self-annealed oligonucleotide CP29 (SEQ ID NO:107) 5′ AATTGCGGCCGC 3′, then digested with NotI and linear purified followed by self-ligation. This procedure introduced a NotI site to pC5LSP, generating pNC5LSP5.

The nucleotide sequence of the wildtype murine p53 gene is presented in FIG. 67 (SEQ ID NO:45). The start codon is at position 1 and the stop codon is at position 1171.

Recombination between donor plasmid pMM148 and ALVAC rescuing virus generated recombinant virus vCP263. vCP263 contains the wild type murine p53 gene under the control of the vaccinia H6 promoter in the C5 locus. Analysis confirms expression.

Insertion of a mutant form of Murine D53 into ALVAC. Plasmid pSVK215 containing a mutant form of the murine p53 gene was received from Arnold Levine (Princeton University, Princeton, N.J.). The mutation in pSVKH215 changes the sequence GTAC of the murine p53 coding sequence (FIG. 67) nt positions 643 through 646 to CCAAGCTTGG. The insertion between nt positions 643 and 646 changes the predicted amino acid coding sequence from val-pro to pro-ser-leu-ala; and the insertion replaces a KpnI site with a HindIII site. The construction of pSVKH215 is described in Tan et al. (1986).

Plasmid pMM136 (described above) contains the vaccinia H6 promoted 5′ end of the p53 gene fused to the 3′ end of the p53 gene in an ALVAC C5 locus insertion plasmid. pMM136 was digested with KspI and XhoI to remove 149 bp, and the 960 bp KspI/XhoI fragment containing the mutation described above from pSVKH215 was inserted. The resultant plasmid, pMM149, contains the H6 promoted murine mutant p53 gene in the C5 locus.

Recombination between donor plasmid pMM149 and ALVAC rescuing virus generated recombinant virus vCP267. vCP267 contains the mutant form of the murine p53 gene under the control of the vaccinia H6 promoter in the C5 locus. Analysis confirms expression.

Example 4.3 Insertion of Mutant Forms of Human P53 into ALVAC and NYVAC

Mutant forms of Human P53 into ALVAC. FIG. 66 (see Example 4.1) presented the sequence of the vaccinia H6 promoted human wild type p53 gene cassette in an ALVAC-based recombinant, vCP207. In this example, to facilitate description of the mutant forms of the human p53 gene being described, FIG. 68 (SEQ ID NO:46) presents only the coding sequence for the human wild type p53 gene. The start codon is at position 1 and the stop codon is at position 1180.

Plasmid Cx22A, containing a mutant form of the human p53 gene, was received from Arnold Levine (Princeton University, Princeton, N.J.). Relative to the wild type p53 sequence presented in FIG. 68, the G at nucleotide position 524 is substituted with an A, changing the arg amino acid at codon 175 of the wild type protein to a his amino acid in Cx22A.

Plasmid pMM110 (see Example 4.1, FIG. 66) contains the vaccinia H6 promoted wildtype human p53 gene in the ALVAC C5 insertion site. The human p53 gene contains two PflmI sites. p53 coding sequences upstream from the first PflmI site and downstream from the second PflmI site are the same in pMM110 as in Cx22A. pMM110 was digested with PflmI to remove the 853 central base pairs of the p53 gene. The 853 bp PflmI fragment from Cx22A containing the base change at position 524 was inserted. The resultant plasmid, pMM143, contains the H6 promoted mutant p53 gene.

Recombination between donor plasmid pMM143 and ALVAC rescuing virus generated recombinant virus vCP270. vCP270 contains the mutant form of the human p53 gene under the control of the vaccinia H6 promoter in the C5 locus.

Plasmid pR4-2 containing a mutant form of the human p53 gene was received from Arnold Levine (Princeton University, Princeton, N.J.). Relative to the wild type p53 sequence presented in FIG. 68, the G at nucleotide position 818 is substituted by an A, changing the arg codon at amino acid position 273 to a his codon in pR4-2.

Plasmid pMM110 (Example 4.1, FIG. 66) contains the vaccinia H6 promoted human wildtype p53 gene in the ALVAC C5 insertion site. p53 coding sequences upstream from the first PflmI site and p53 coding sequences downstream from the second PflmI site are the same in pMM110 as in pR4-2. pMM110 was digested with PflmI to remove the 853 central base pairs of the p53 gene. The 853 bp PflmI fragment from pR4-2 containing the base change at nucleotide position 818 was inserted. The resultant plasmid, pMM144, contains the H6 promoted mutant form of the human p53 gene in the C5 insertion locus.

Recombination between donor plasmid pMM144 and ALVAC rescuing virus generated recombinant virus vCP269. vCP269 contains the mutant form of the human p53 gene under the control of the vaccinia H6 promoter in the C5 locus.

Mutant forms of Human p53 into NYVAC. Plasmid Cx22A, described above, contains a mutant form of the human p53 gene, in which the G at nucleotide position 524 (FIG. 68) is substituted by an A, changing the arg codon at amino acid position 175 to a his codon in Cx22A.

Plasmid pMM106 (Example 4.1) contains the vaccinia H6 promoted wild-type human p53 gene in the NYVAC I4L insertion locus. p53 coding sequences upstream from the first PflmI site and p53 coding sequences downstream from the second PflmI site are the same in pMM106 as in Cx22A. pMM106 was digested with PflmI to remove the 853 central base pairs of the p53 gene. The 853 bp PflmI fragment from Cx22A containing the base change at position 524 was inserted. The resultant plasmid, pMM140, contains the H6 promoted mutant p53 gene.

Recombination between donor plasmid pMM140 and NYVAC rescuing virus generated recombinant virus vP1234. vP1234 contains the mutant form of the human p53 gene under the control of the vaccinia H6 promoter in the I4L locus.

Plasmid pR4-2, described above, contains a mutant form of the human p53 gene, in which the G at nucleotide position 818 (FIG. 68) is substituted by an A, changing the arg codon at amino acid position 273 to a his codon in pR4-2. pMM106 (Example 4.1) contains the H6 promoted wild-type human p53 gene in the I4L locus. p53 coding sequences upstream from the first PflmI site and p53 coding sequences downstream from the second PflmI site are the same in pMM106 as in pR4-2. pMM106 was digested with PflmI to remove the 853 central base pairs of the p53 gene. The 853 bp PflmI fragment from pR4-2 containing the base change at position 818 was inserted. The resultant plasmid, pMM141, contains the H6 promoted mutant p53 gene.

Recombination between donor plasmid pMM141 and NYVAC rescuing virus generated recombinant virus vP1233. vP1233 contains the mutant form of the human p53 gene under the control of the vaccinia H6 promoter in the I4L locus.

A listing of the wildtype and mutant forms of murine p53 and the mutant forms of human p53 present in ALVAC and NYVAC recombinants described in Examples 4.2 and 4.3 is provided in Table 15.

TABLE 15 Recombinant Virus Parent Virus Species Gene Insert vCP263 ALVAC murine w.t. p53 vCP267 ALVAC murine p53 (+3 aa) vCP270 ALVAC human p53 (aa 175; R to H) vCP269 ALVAC human p53 (aa 273; R to H) vP1234 NYVAC human p53 (aa 175; R to H) vP1233 NYVAC human p53 (aa 273; R to H)

Immunoprecipitation. ALVAC and NYVAC based recombinants vP1101, vP1096, vP1098, vCP207, vCP193, vCP191 (all described in Example 4.1; Table 14, as well as ALVAC and NYVAC based recombinants vCP270, vCP269, vP1233, vP1234 described in this Example, Table 15), contain wild type or mutant forms of the human p53 gene. All of these recombinant virus were assayed for expression of the human p53 gene using immunoprecipitation.

Recombinant or parental virus were inoculated onto preformed monolayers of tissue culture cells in the presence of radiolabelled ³⁵S-methionine and treated as previously described (Taylor et al., 1990). Immunoprecipitation reactions were performed using a human p53 specific monoclonal antibody 1801. A protein of between 47 and 53 kDa was precipitated from cells infected with any of the recombinant viruses, vP1101, vP1096, vP1098, vCP207, vCP193, vCP191, vCP270, vCP269, vP1233, or vP1234, but not from uninfected cells or cells infected with parental ALVAC or NYVAC virus.

Based upon the properties of the poxvirus vector systems, NYVAC, ALVAC and TROVAC cited above, such vectors expressing either wildtype or mutant forms of p53 provide valuable reagents to determine whether endogenous CTL activities can be detected in patient effector populations (TILS, PBMC, or lymph node cells); and, valuable vehicles for the stimulation or the augmenting of such activities; for instance, augmenting such activities by in vitro or ex vivo stimulation with these recombinant viruses. Further, the highly attenuated properties of both NYVAC and ALVAC allow the recombinants of the invention to be used for interventive immunotherapeutic modalities discussed above, e.g., in vivo interventive immunotherapy.

Example 5 Poxvirus-Rat CMV IE1 and IE2 Recombinants

Plasmids RCMVIE1 and RCMVIE2 were obtained from Dr. Toren Finkel (NIH-NHLBI), and transformed into bacteria MN522 (available from Stratgene). In FIG. 69 RCMVIE1 the coding sequence for the Rat CMV IE1 gene is depicted from nucleotides 443-2140 (SEQ ID NO:47). In FIG. 70 RCMVIE2 the coding sequence for the Rat CMV IE1 gene is depicted from nucleotides 443-2002 (SEQ ID NO:48).

Oligonucleotides SPIE1C (5′-TAG-ATA-AAG-CTG-CAG-AGT-CA-3′) (SEQ ID NO:176) and SPIE1D (5′-AGA-CTC-GAG-ATA-AAA-ATT-ATG-ATC-TCC-TGC-CTC-TCT-3′) (SEQ ID NO:177) were used in PCR with plasmid RCMVIE1 to generate a 585 bp fragment containing the C-terminal end of the IE1 gene. This fragment was digested with PstI and XhoI (yielding a 565 bp fragment) and cloned into BamHI/XhoI digested and alkaline phosphatase treated IBI25 along with a 1132 bp BamHI/PstI fragment from RCMVIE1 generating plasmid IE1-2-21.

Oligonucleotides SPIE2C (5′-CGC-AAG-CTT-CGC-GAT-AAA-AAT-TAT-TCT-GAA-TCG-GAG-TCC-T-3′) (SEQ ID NO:178) and SPIE2D (5′-ATG-ATA-ATC-CAA-GCG-GCA-ACA-3′) (SEQ ID NO:179) were used in PCR with plasmid RCMVIE2 to generate a 272 bp fragment containing the C-terminal end of the IE2 gene. This fragment was digested with NsiI and PstI (yielding a 210 bp fragment) and cloned into BamHI/HindIII digested IBI25 along with a 1361 bp BamHI/NsiII fragment from RCMVIE2 generating plasmid IE2-2-4.

Plasmid IBI25 was digested with EcoRI and XbaI, treated with alkaline phosphatase and ligated to kinased and annealed oligonucleotides SPIE2A (5′-CTA-GAG-GAT-CCA-TTT-TAT-ATT-GTA-ATT-ATA-TAT-TTT-CAA-TTT-TGA-AAT-CCC-AAA-ACC-CGG-GAG-ATC-TG-3′) (SEQ ID NO:180) and SPIE2B (5′-AAT-TCA-GAT-CTC-CCG-GGT-TTT-GGG-ATT-TCA-AAA-TTG-AAA-ATA-TAT-AAT-TAC-AAT-ATA-AAA-TGG-ATC-CT-3′) (SEQ ID NO:181) yielding plasmid IE2-1-1.

Plasmid IE2-1-1 was digested with BamHI and HindIII, treated with alkaline phosphatase and ligated to a 1570 bp BamHI/HindIII fragment derived from plasmid IE2-2-4 yielding plasmid IE2-3-1 which contains the Rat CMV IE2 gene under the control of the entemopoxvirus 42K early promoter.

NYVAC donor plasmid pSD553 (which contains the K1L host range gene, a polylinker and sequences flanking the ATI locus; see U.S. Pat. No. 5,494,807) was digested with BamHI and NruI, treated with alkaline phosphatase and ligated to a 1618 bp BglII/NruI fragment from plasmid IE2-3-1 generating plasmid IE2-4-16.

Plasmid MCP1-3 (which contains the vaccinia early/late H6 promoter) was derived from SPHA-H6. Plasmid SPHA-H6 was used in PCR with oligonucleotides SPMCP1 (5′-GCCTCTAGACTCGAGCGCCGACCAGTTCTCCATTACGATACAAACTTAACGGATATC-3′) (SEQ ID NO:184) and SPMCP2 (5′-CGCGAATTCTTCTTTATTCTATACTTA-3′) (SEQ ID NO:185) and the resulting 166 bp fragment was digested with Eco RI and XbaI and ligated to EcoRI/XbaI digested and alkaline phosphatase-treated IBI24 generating plasmid MCP1-3.

Plasmid MCP1-3 was digested with EcoRV (within the H6 promoter) and XbaI (within the polylinker), treated with alkaline phosphatase and ligated to kinased and annealed oligonucleotides SPIE1A (5′-ATC-CGT-TAA-GTT-TGT-ATC-GTA -ATG-GAT-CCT-3′) (SEQ ID NO:182) and SPIE1B (5′-CTA-GAG-GAT-CCA-TTA-CGA-TAC-AAA-CTT-AAC-GGA-T-3′) (SEQ ID NO:183) yielding plasmid IE1-1-3.

Plasmid IE1-1-3 was digested with BamHI and XhoI, treated with alkaline phosphatase and ligated to a 1703 bp BamHI/XhoI fragment from plasmid IE1-2-21 yielding plasmid IE1-3-2 (which contains the Rat CMV IE1 gene under the control of the vaccinia H6 promoter).

Plasmid IE2-4-16 was digested with SmaI and XhoI and treated with alkaline phosphatase. Plasmid IE1-3-2 was digested with EcoRI, filled in with Klenow, digested with XhoI and a 1838 bp fragment isolated. Ligation of these two fragments yielded plasmid COPAKIE1.2-2. The DNA sequence of Rat CMV IE1 and IE2 plus additional flanking DNA sequences in plasmid COPAKIE1.2-2 is shown in FIGS. 71A and B providing the nucleotide sequence (DNA) of COPIE1₁₃ 2 (SEQ ID NO:49). The H6 promoted Rat CMV IE1 gene is located between nucleotides 2252 and 431. The 42K promoted Rat CMV IE2 gene is located between nucleotides 2261 and 3862.

Plasmid COPAKIE1.2-2 was transfected into NYVAC infected CEF cells to generate recombinant vP1479. Analysis confirms expression.

Example 6 Baculovirus Rat CMV IE1 OR IE2 Recombinants

Baculovirus recombinants expressing Rat CMV IE1 or IE2 were derived using the BAC-TO-BAC BACULOVIRUS EXPRESSION SYSTEM (Life technologies) as described in the instruction manual. This system is based on the site specific transposition of an expression cassette into a baculovirus shuttle vector (bacmid) propagated in E. coli. The recombinant bacmid DNA is isolated and used to transfect insect cells. Viral stocks harvested from transfected cells are amplified and used to infect insect cells for subsequent protein expression, purification (by virtue of the His tag present on the recombinant protein) and analysis (see FIG. 72, Generation of recombinant baculovirus and gene expression with the Bac-to-Bac Expression system).

The donor plasmid pFASTBACHTa (FIG. 73) was digested within the multiple cloning sites (FIG. 74) with BamHI and HindIII and a 4771 bp fragment isolated. Plasmid IE1-2-21 was digested with BamHI and HindIII and a 1716 bp fragment isolated. Ligation of these two fragments yielded plasmid BacRIE1-3 which encodes a fusion protein containing 25 amino acids derived from pFASTBACHTa and the entire rat CMV IE1 amino acid sequence.

Plasmid IE2-2-4 was digested with BamHI and HindIII and a 1570 bp fragment was isolated and ligated to the 4771 bp BamHI/HindIII fragment from pFASTBACHTa yielding plasmid BacRIE2-4. This plasmid encodes a fusion protein containing 25 amino acids derived from pFASTBACHTa and the entire rat CMV IE2 amino acid sequence.

BacRIE1-3 and BacRIE2-4 were transformed into DH10Bac cells and transposition allowed to occur. Recombinant bacmid DNA was isolated from appropriate colonies and used to transfect Sf9 insect cells to generate recombinant baculoviruses A6 (Rat CMV IE1 recombinant) and B2 (Rat CMV IE2 recombinant). Analysis confirms expression (FIG. 76A, lane 6).

FIG. 75 (SEQ ID NO: 50) provides the nucleotide sequence (DNA) of HCMV IE2, which is useful in generating vectors or recombinants for use in this invention.

Proteins expressed by the recombinant baculovirus were isolated and purified as follows:

Purification of Recombinant Proteins Expressed by Baculovirus

Baculovirus proteins were purified using the His Trap chelating column from Pharmacia Biotech. A suspension culture of SF9 insect cells at a density of 2×10⁶ per ml was inoculated with recombinant baculovirus at a multiplicity of 1 plaque forming unit of virus per cell. Cells were incubated at 28° and harvested at 72 hours post infection. Cells were spun out at 2000 rpm for 10 minutes at 4° C. and stored at −80° C. until processing. Cells were lysed using 5 ml of lysis buffer per gram of cells. Lysis buffer was composed of 1×Phosphate buffer (supplied with kit), 10 mM Imidazole (supplied with kit), 1% NP-40, 1 mM PMSF, and 0.01M Mercaptoethanol. Cells were sonicated to release the virus and spun out at 8000 rpm for 10 minutes, 4° C. The supernatant was filtered through a 0.45 micron disc filter to remove particulates. The column was prepared for use by washing with 5 ml water and charging with 0.5 ml 0.1M nickel salt solution (supplied with kit); this was followed by a 5 ml water wash. The column was equilibrated with 10 ml of the lysis buffer prior to loading. The sample was applied to the column at a flow rate of 1 ml per minute. Next, the column was washed with 10 ml of lysis buffer. Fractions were eluted with a buffer composed of 1×Phosphate, 500 mM Imidazole, 10% NP-40, 0.01M Mercaptoethanol in 1 ml aliquots. Fractions were tested by Western Blot using an ECL kit. The primary antiserum was Rabbit anti Rat Cytomegalovirus IE1 and IE2 specific serum from Gordon Sandford, Johns Hopkins at a 1:300 dilution in PBS containing 1% Tween (such serum can be generated by the skilled artisan from isolation of native IE1 and IE2). The conjugate used was an HRP swine anti rabbit (DAKO) at 1:1000. Positive fractions were pooled and dialyzed against PBS (Spectra/Por 1 6,000-8,000 dialysis membrane). Protein determinations were made using the BCA microtiter plate method and samples were examined for purity by Coomassie Blue stain and Western Blot.

FIGS. 76A and B, respectively, show Western Blot and Coomassie Blue stained gel. In FIG. 76A: lane 1=SF9 insect cell lysate, lane 2=baculovirus RCMVIE1 infected SF9 cell lysate, lane 3=RCMVIE1 purified protein preparation, lane 4=baculovirus RCMVIE2 infected SF9 cell lysate, lane 5=RK-13 cells, lane 6=vP1479 infected RK-13 cell lysate, and lane 7=prestained molecular weight markers. In FIG. 76B: lane 1=RCMVIE1 purified protein preparation, and lane 2=prestained molecular weight markers.

Example 7 Additional Baculovirus Recombinants

By employing the techniques of Smith et al., U.S. Pat. No. 4,745,051, incorporated herein by reference, or of other literature concerning baculovirus recombinants, including the techniques of Example 6, with exogenous DNA of any of U.S. Pat. Nos. 5,047,320, 5,075,213, Paoletti, U.S. Pat. No. 5,338,683, Paoletti et al., U.S. Pat. No. 5,494,807, Paoletti et al., PCT publication WO 96/39491, based on U.S. applications Ser. Nos. 08/471,014, filed Jun. 6, 1995, and 08/658,665, filed Jun. 5, 1995 (see Example 3), Paoletti et al. WO 94/16716 based on U.S. applications Ser. Nos. 007,115, filed Jan. 21, 1993, and 184,009, filed Jan. 19, 1994 (see Example 4), or other documents cited and incorporated herein, or literature concerning HCMV antigens, epitopes of interest, p53, p53 epitopes of interest, and DNA coding therefor, baculovirus embodiments expressing any desired HCMV and/or p53 epitope of interest, including those set forth in Examples 3 and 4 for various HCMV epitopes of interest and p53 epitopes of interest, and gene products therefrom, are obtained, for practice of this invention. Analysis confirms expression.

Example 8 Adenovirus Recombinants

By employing the techniques of U.S. Pat. Nos. 5,591,439 and 5,552,143, or of other literature concerning adenovirus recombinants with exogenous DNA of any of U.S. Pat. Nos. 5,047,320, 5,075,213, Paoletti, U.S. Pat. No. 5,338,683, Paoletti et al., U.S. Pat. No. 5,494,807, Paoletti et al., PCT publication WO 96/39491, based on U.S. applications Ser. Nos. 08/471,014, filed Jun. 6, 1995, and 08/658,665, filed Jun. 5, 1995 (see Example 3), Paoletti et al. WO 94/16716 based on U.S. applications Ser. Nos. 007,115, filed Jan. 21, 1993, and 184,009, filed Jan. 19, 1994 (see Example 4), or other documents cited and incorporated herein, or literature concerning HCPV antigens, epitopes of interest, p53, p53 epitopes of interest, and DNA coding therefor, adenovirus embodiments expressing any desired HCMV and/or p53 epitope of interest, including the HCMV and p53 epitopes of interest of Examples 3 and 4 are obtained, for practice of this invention. Analysis confirms expression.

Example 9 DNA Expression System Embodiments

By employing the techniques of U.S. Pat. Nos. 5,591,639, 5,589,466, 5,580,589, incorporated herein by reference, or of other literature concerning DNA expression vectors with exogenous DNA of any of U.S. Pat. Nos. 5,047,320, 5,075,213, Paoletti, U.S. Pat. No. 5,338,683, Paoletti et al., U.S. Pat. No. 5,494,807, Paoletti et al., PCT publication WO 96/39491, based on U.S. applications Ser. Nos. 08/471,014, filed Jun. 6, 1995, and 08/658,665, filed Jun. 5, 1995 (see Example 3), Paoletti et al. WO 94/16716 based on U.S. applications Ser. Nos. 007,115, filed Jan. 21, 1993, and 184,009, filed Jan. 19, 1994 (see Example 4), or other documents cited and incorporated herein or literature concerning HCMV antigens, epitopes of interest, p53, p53 epitopes of interest, and DNA coding therefor, DNA expression vector embodiments expressing any desired HCMV and/or p53 epitope of interest, including HCMV and p53 epitopes as in Examples 3 and 4 and gene products therefrom, are obtained, for practice of this invention. Analysis confirms expression.

Example 10 Formulations and Use

Native HCMV epitopes are obtained from cells infected with HCMV, and native p53 epitopes are also obtained from cells wherein expression thereof is detected. Recombinant HCMV and p53 epitopes are obtained from recombinants expressing these products, e.g., as in the previous Examples. These proteins are admixed with carrier, diluent etc., as herein described in amounts as herein described to obtain formulations. Recombinants and DNA expression systems expressing HCMV epitopes and p53 epitopes are obtained, e.g., as in the previous Examples; and, these recombinants and DNA expression systems are admixed with carrier, diluent, etc., as herein described to obtain formulations. Patients are administered the formulations as herein described for the prevention and/or treatment of vascular disease such as atherosclerosis and/or restenosis, including in a manner analogous to gene therapy directed against SMC proliferation, as described in literature cited herein. Propensity towards or against such disease is determined using diagnostic methods as herein described.

Having thus described in detail preferred embodiments of the present invention, it is to be understood that the invention defined by the appended claims is not to be limited by particular details set forth in the above description as many apparent variations thereof are possible without departing from the spirit or scope thereof.

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184 2724 base pairs nucleic acid single linear DNA (genomic) unknown 1 ATGGAATCCA GGATCTGGTG CCTGGTAGTC TGCGTTAACT TGTGTATCGT CTGTCTGGGT 60 GCTGCGGTTT CCTCATCTTC TACTCGTGGA ACTTCTGCTA CTCACAGTCA CCATTCCTCT 120 CATACGACGT CTGCTGCTCA TTCTCGATCC GGTTCAGTCT CTCAACGCGT AACTTCTTCC 180 CAAACGGTCA GCCATGGTGT TAACGAGACC ATCTACAACA CTACCCTCAA GTACGGAGAT 240 GTGGTGGGGG TCAACACCAC CAAGTACCCC TATCGCGTGT GTTCTATGGC ACAGGGTACG 300 GATCTTATTC GCTTTGAACG TAATATCGTC TGCACCTCGA TGAAGCCCAT CAATGAAGAC 360 CTGGACGAGG GCATCATGGT GGTCTACAAA CGCAACATCG TCGCGCACAC CTTTAAGGTA 420 CGAGTCTACC AGAAGGTTTT GACGTTTCGT CGTAGCTACG CTTACATCCA CACCACTTAT 480 CTGCTGGGCA GCAACACGGA ATACGTGGCG CCTCCTATGT GGGAGATTCA TCATATCAAC 540 AGTCACAGTC AGTGCTACAG TTCCTACAGC CGCGTTATAG CAGGCACGGT TTTCGTGGCT 600 TATCATAGGG ACAGCTATGA AAACAAAACC ATGCAATTAA TGCCCGACGA TTATTCCAAC 660 ACCCACAGTA CCCGTTACGT GACGGTCAAG GATCAATGGC ACAGCCGCGG CAGCACCTGG 720 CTCTATCGTG AGACCTGTAA TCTGAATTGT ATGGTGACCA TCACTACTGC GCGCTCCAAG 780 TATCCCTATC ATTTTTTCGC AACTTCCACG GGTGATGTGG TTGACATTTC TCCTTTCTAC 840 AACGGAACTA ATCGCAATGC CAGCTATTTT GGAGAAAACG CCGACAAGTT TTTCATTTTT 900 CCGAACTACA CTATCGTCTC CGACTTTGAA AGACCGAATT CTGCGTTAGA GACCCACAGG 960 TTGGTGGCTT TTCTTGAACG TGCGGACTCA GTGATCTCCT GGGATATACA GGACGAGAAG 1020 AATGTTACTT GTCAACTCAC TTTCTGGGAA GCCTCGGAAC GCACCATTCG TTCCGAAGCC 1080 GAGGACTCGT ATCACTTTTC TTCTGCCAAA ATGACCGCCA CTTTCTTATC TAAGAAGCAA 1140 GAGGTGAACA TGTCCGACTC TGCGCTGGAC TGTGTACGTG ATGAGGCCAT AAATAAGTTA 1200 CAGCAGATTT TCAATACTTC ATACAATCAA ACATATGAAA AATATGGAAA CGTGTCCGTC 1260 TTTGAAACCA CTGGTGGTTT GGTGGTGTTC TGGCAAGGTA TCAAGCAAAA ATCTCTGGTG 1320 GAACTCGAAC GTTTGGCCAA CCGCTCCAGT CTGAATCTTA CTCATAATAG AACCAAAAGA 1380 AGTACAGATG GCAACAATGC AACTCATTTA TCCAACATGG AGTCGGTGCA CAATCTGGTC 1440 TACGCCCAGC TGCAGTTCAC CTATGACACG TTGCGCGGTT ACATCAACCG GGCGCTGGCC 1500 GAAATCGCAG AAGCCTGGTG TGTGGATCAA CGGCGCACCC TAGAGGTCTT CAAGGAACTT 1560 AGCAAGATCA ACCCGTCAGC TATTCTCTCG GCCATCTACA ACAAACCGAT TGCCGCGCGT 1620 TTCATGGGTG ATGTCCTGGG TCTGGCCAGC TGCGTGACCA TTAACCAAAC CAGCGTCAAG 1680 GTGCTGCGTG ATATGAATGT GAAGGAATCG CCAGGACGCT GCTACTCACG ACCAGTGGTC 1740 ATCTTTAATT TCGCCAACAG CTCGTACGTG CAGTACGGTC AACTGGGCGA GGATAACGAA 1800 ATCCTGTTGG GCAACCACCG CACTGAGGAA TGTCAGCTTC CCAGCCTCAA GATCTTCATC 1860 GCCGGCAACT CGGCCTACGA GTACGTGGAC TACCTCTTCA AACGCATGAT TGACCTCAGC 1920 AGCATCTCCA CCGTCGACAG CATGATCGCC CTAGACATCG ACCCGCTGGA AAACACCGAC 1980 TTCAGGGTAC TGGAACTTTA CTCGCAGAAA GAATTGCGTT CCAGCAACGT TTTTGATCTC 2040 GAGGAGATCA TGCGCGAGTT CAATTCGTAT AAGCAGCGGG TAAAGTACGT GGAGGACAAG 2100 GTAGTCGACC CGCTGCCGCC CTACCTCAAG GGTCTGGACG ACCTCATGAG CGGCCTGGGC 2160 GCCGCGGGAA AGGCCGTTGG CGTAGCCATT GGGGCCGTGG GTGGCGCGGT GGCCTCCGTG 2220 GTCGAAGGCG TTGCCACCTT CCTCAAAAAC CCCTTCGGAG CCTTCACCAT CATCCTCGTG 2280 GCCATAGCCG TCGTCATTAT CATTTATTTG ATCTATATCC GACAGCGGCG TCTCTGCATG 2340 CAGCCGCTGC AGAACCTCTT TCCCTATCTG GTGTCCGCCG ACGGGACCAC CGTGACGTCG 2400 GGCAACACCA AAGACACGTC GTTACAGGCT CCGCCTTCCT ACGAGGAAAG TGTTTATAAT 2460 TCTGGTCGCA AAGGACCGGG ACCACCGTCG TCTGATGCAT CCACGGCGGC TCCGCCTTAC 2520 ACCAACGAGC AGGCTTACCA GATGCTTCTG GCCCTGGTCC GTCTGGACGC AGAGCAGCGA 2580 GCGCACGAGA ACGGTACAGA TTCTTTGGAC GGACAGACTG GCACGCAGGA CAAGGGACAG 2640 AAGCCCAACC TGCTAGACCG ACTGCGACAC CGCAAAAACG GCTACCGACA CTTGAAAGAC 2700 TCCGACGAAG AAGAGAACGT CTGA 2724 4260 base pairs nucleic acid single linear DNA (genomic) unknown 2 AAGCTTTTGC GATCAATAAA TGGATCACAA CCAGTATCTC TTAACGATGT TCTTCGCAGA 60 TGATGATTCA TTTTTTAAGT ATTTGGCTAG TCAAGATGAT GAATCTTCAT TATCTGATAT 120 ATTGCAAATC ACTCAATATC TAGACTTTCT GTTATTATTA TTGATCCAAT CAAAAAATAA 180 ATTAGAAGCC GTGGGTCATT GTTATGAATC TCTTTCAGAG GAATACAGAC AATTGACAAA 240 ATTCACAGAC TCTCAAGATT TTAAAAAACT GTTTAACAAG GTCCCTATTG TTACAGATGG 300 AAGGGTCAAA CTTAATAAAG GATATTTGTT CGACTTTGTG ATTAGTTTGA TGCGATTCAA 360 AAAAGAATCC TCTCTAGCTA CCACCGCAAT AGATCCTATT AGATACATAG ATCCTCGTCG 420 CGATATCGCA TTTTCTAACG TGATGGATAT ATTAAAGTCG AATAAAGTGA ACAATAATTA 480 ATTCTTTATT GTCATCATGT AATTAACTAG CTACCCGGGA GATCTCTCGA GCTGCAGAAG 540 CTTATAAAAA TCACAAGTCT CTGTCACTTT TTTTGTCTAG TTTTTTTTTC TCCTCTTGGT 600 TCAGACGTTC TCTTCTTCGT CGGAGTCTTT CAAGTGTCGG TAGCCGTTTT TGCGGTGTCG 660 CAGTCGGTCT AGCAGGTTGG GCTTCTGTCC CTTGTCCTGC GTGCCAGTCT GTCCGTCCAA 720 AGAATCTGTA CCGTTCTCGT GCGCTCGCTG CTCTGCGTCC AGACGGACCA GGGCCAGAAG 780 CATCTGGTAA GCCTGCTCGT TGGTGTAAGG CGGAGCCGCC GTGGATGCAT CAGACGACGG 840 TGGTCCCGGT CCTTTGCGAC CAGAATTATA AACACTTTCC TCGTAGGAAG GCGGAGCCTG 900 TAACGACGTG TCTTTGGTGT TGCCCGACGT CACGGTGGTC CCGTCGGCGG ACACCAGATA 960 GGGAAAGAGG TTCTGCAGCG GCTGCATGCA GAGACGCCGC TGTCGAGTAT AGATCAAATA 1020 AATGATAATG ACGACGGCTA TGGCCACGAG GATGATGGTG AAGGCTCCGA AGGGGTTTTT 1080 GAGGAAGGTG GCAACGCCTT CGACCACGGA GGCCACCGCG CCACCCACGG CCCCAATGGC 1140 TACGCCAACG GCCTTTCCCG CGGCGCCCAG GCCGCTCATG AGGTCGTCCA GACCCTTGAG 1200 GTAGGGCGGC AGCGGGTCGA CTACCTTGTC CTCCACGTAC TTTACCCGCT GCTTATACGA 1260 ATTGAACTCG CGCATGATCT CCTCGAGATC AAAAACGTTG CTGGAACGCA ATTCTTTCTG 1320 CGAGTAAAGT TCCAGTACCC TGAAGTCGGT GTTTTCCAGC GGGTCGATGT CTAGGGCGAT 1380 CATGCTGTCG ACGGTGGAGA TGCTGCTGAG GTCAATCATG CGTTTGAAGA GGTAGTCCAC 1440 GTACTCGTAG GCCGAGTTGC CGGCGATGAA GATCTTGAGG CTGGGAAGCT GACATTCCTC 1500 AGTGCGGTGG TTGCCCAACA GGATTTCGTT ATCCTCGCCC AGTTGACCGT ACTGCACGTA 1560 CGAGCTGTTG GCGAAATTAA AGATGACCAC TGGTCGTGAG TAGCAGCGTC CTGGCGATTC 1620 CTTCACATTC ATATCACGCA GCACCTTGAC GCTGGTTTGG TTAATGGTCA CGCAGCTGGC 1680 CAGACCCAGG ACATCACCCA TGAAACGCGC GGCAATCGGT TTGTTGTAGA TGGCCGAGAG 1740 AATAGCTGAC GGGTTGATCT TGCTAAGTTC CTTGAAGACC TCTAGGGTGC GCCGTTGATC 1800 CACACACCAG GCTTCTGCGA TTTCGGCCAG CGCCCGGTTG ATGTAACCGC GCAACGTGTC 1860 ATAGGTGAAC TGCAGCTGGG CGTAGACCAG ATTGTGCACC GACTCCATGT TGGATAAATG 1920 AGTTGCATTG TTGCCATCTG TACTTCTTTT GGTTCTATTA TGAGTAAGAT TCAGACTGGA 1980 GCGGTTGGCC AAACGTTCGA GTTCCACCAG AGATTTTTGC TTGATACCTT GCCAGAACAC 2040 CACCAAACCA CCAGTGGTTT CAAAGACGGA CACGTTTCCA TATTTTTCAT ATGTTTGATT 2100 GTATGAAGTA TTGAAAATCT GCTGTAACTT ATTTATGGCC TCATCACGTA CACAGTCCAG 2160 CGCAGAGTCG GACATGTTCA CCTCTTGCTT CTTAGATAAG AAAGTGGCGG TCATTTTGGC 2220 AGAAGAAAAG TGATACGAGT CCTCGGCTTC GGAACGAATG GTGCGTTCCG AGGCTTCCCA 2280 GAAAGTGAGT TGACAAGTAA CATTCTTCTC GTCCTGTATA TCCCAGGAGA TCACTGAGTC 2340 CGCACGTTCA AGAAAAGCCA CCAACCTGTG GGTCTCTAAC GCAGAATTCG GTCTTTCAAA 2400 GTCGGAGACG ATAGTGTAGT TCGGAAAAAT GAAAAACTTG TCGGCGTTTT CTCCAAAATA 2460 GCTGGCATTG CGATTAGTTC CGTTGTAGAA AGGAGAAATG TCAACCACAT CACCCGTGGA 2520 AGTTGCGAAA AAATGATAGG GATACTTGGA GCGCGCAGTA GTGATGGTCA CCATACAATT 2580 CAGATTACAG GTCTCACGAT AGAGCCAGGT GCTGCCGCGG CTGTGCCATT GATCCTTGAC 2640 CGTCACGTAA CGGGTACTGT GGGTGTTGGA ATAATCGTCG GGCATTAATT GCATGGTTTT 2700 GTTTTCATAG CTGTCCCTAT GATAAGCCAC GAAAACCGTG CCTGCTATAA CGCGGCTGTA 2760 GGAACTGTAG CACTGACTGT GACTGTTGAT ATGATGAATC TCCCACATAG GAGGCGCCAC 2820 GTATTCCGTG TTGCTGCCCA GCAGATAAGT GGTGTGGATG TAAGCGTAGC TACGACGAAA 2880 CGTCAAAACC TTCTGGTAGA CTCGTACCTT AAAGGTGTGC GCGACGATGT TGCGTTTGTA 2940 GACCACCATG ATGCCCTCGT CCAGGTCTTC ATTGATGGGC TTCATCGAGG TGCAGACGAT 3000 ATTACGTTCA AAGCGAATAA GATCCGTACC CTGACCCATA GAACACACGC GATAGGGGTA 3060 CTTGGTGGTG TTGACCCCCA CCACATCTCC GTACTTGAGG GTAGTGTTGT AGATGGTCTC 3120 GTTAACACCA TGGCTGACCG TTTGGGAAGA AGTTACGCGT TGAGAGACTG AACCGGATCG 3180 AGAATGAGCA GCAGACGTCG TATGAGAGGA ATGGTGACTG TGAGTAGCAG AAGTTCCACG 3240 AGTAGAAGAT GAGGAAACCG CAGCACCCAG ACAGACGATA CACAAGTTAA CGCAGACTAC 3300 CAGGCACCAG ATCCTGGATT CCATTACGAT ACAAACTTAA CGGATATCGC GATAATGAAA 3360 TAATTTATGA TTATTTCTCG CTTTCAATTT AACACAACCC TCAAGAACCT TTGTATTTAT 3420 TTTCACTTTT AAGTATAGAA TAAAGAAGCT TGCATGCCAC GCGTCTCGAG GGCCCCTGCA 3480 GGTCGACTCT AGAGGATCCT GATCCTTTTT CTGGGTAAGT AATACGTCAA GGAGAAAACG 3540 AAACGATCTG TAGTTAGCGG CCGCCTAATT AACTAATATT ATATTTTTTA TCTAAAAAAC 3600 TAAAAATAAA CATTGATTAA ATTTTAATAT AATACTTAAA AATGGATGTT GTGTCGTTAG 3660 ATAAACCGTT TATGTATTTT GAGGAAATTG ATAATGAGTT AGATTACGAA CCAGAAAGTG 3720 CAAATGAGGT CGCAAAAAAA CTGCCGTATC AAGGACAGTT AAAACTATTA CTAGGAGAAT 3780 TATTTTTTCT TAGTAAGTTA CAGCGACACG GTATATTAGA TGGTGCCACC GTAGTGTATA 3840 TAGGATCGGC TCCTGGTACA CATATACGTT ATTTGAGAGA TCATTTCTAT AATTTAGGAA 3900 TGATTATCAA ATGGATGCTA ATTGACGGAC GCCATCATGA TCCTATTTTA AATGGATTGC 3960 GTGATGTGAC TCTAGTGACT CGGTTCGTTG ATGAGGAATA TCTACGATCC ATCAAAAAAC 4020 AACTGCATCC TTCTAAGATT ATTTTAATTT CTGATGTGAG ATCCAAACGA GGAGGAAATG 4080 AACCTAGTAC GGCGGATTTA CTAAGTAATT ACGCTCTACA AAATGTCATG ATTAGTATTT 4140 TAAACCCCGT GGCGTCTAGT CTTAAATGGA GATGCCCGTT TCCAGATCAA TGGATCAAGG 4200 ACTTTTATAT CCCACACGGT AATAAAATGT TACAACCTTT TGCTCCTTCA TATTCAGCTG 4260 7351 base pairs nucleic acid single linear DNA (genomic) unknown 3 AGATATTTGT TAGCTTCTGC CGGAGATACC GTGAAAATCT ATTTTCTGGA AGGAAAGGGA 60 GGTCTTATCT ATTCTGTCAG CAGAGTAGGT TCCTCTAATG ACGAAGACAA TAGTGAATAC 120 TTGCATGAAG GTCACTGTGT AGAGTTCAAA ACTGATCATC AGTGTTTGAT AACTCTAGCG 180 TGTACGAGTC CTTCTAACAC TGTGGTTTAT TGGCTGGAAT AAAAGGATAA AGACACCTAT 240 ACTGATTCAT TTTCATCTGT CAACGTTTCT CTAAGAGATT CATAGGTATT ATTATTACAT 300 CGATCTAGAA GTCTAATAAC TGCTAAGTAT ATTATTGGAT TTAACGCGCT ATAAACGCAT 360 CCAAAACCTA CAAATATAGG AGAAGCTTCT CTTATGAAAC TTCTTAAAGC TTTACTCTTA 420 CTATTACTAC TCAAAAGAGA TATTACATTA ATTATGTGAT GAGGCATCCA ACATATAAAG 480 AAGACTAAAG CTGTAGAAGC TGTTATGAAG AATATCTTAT CAGATATATT AGATGCATTG 540 TTAGTTCTGT AGATCAGTAA CGTATAGCAT ACGAGTATAA TTATCGTAGG TAGTAGGTAT 600 CCTAAAATAA ATCTGATACA GATAATAACT TTGTAAATCA ATTCAGCAAT TTCTCTATTA 660 TCATGATAAT GATTAATACA CAGCGTGTCG TTATTTTTTG TTACGATAGT ATTTCTAAAG 720 TAAAGAGCAG GAATCCCTAG TATAATAGAA ATAATCCATA TGAAAAATAT AGTAATGTAC 780 ATATTTCTAA TGTTAACATA TTTATAGGTA AATCCAGGAA GGGTAATTTT TACATATCTA 840 TATACGCTTA TTACAGTTAT TAAAAATATA CTTGCAAACA TGTTAGAAGT AAAAAAGAAA 900 GAACTAATTT TACAAAGTGC TTTACCAAAA TGCCAATGGA AATTACTTAG TATGTATATA 960 ATGTATAAAG GTATGAATAT CACAAACAGC AAATCGGCTA TTCCCAAGTT GAGAAACGGT 1020 ATAATAGATA TATTTCTAGA TACCATTAAT AACCTTATAA GCTTGACGTT TCCTATAATG 1080 CCTACTAAGA AAACTAGAAG ATACATACAT ACTAACGCCA TACGAGAGTA ACTACTCATC 1140 GTATAACTAC TGTTGCTAAC AGTGACACTG ATGTTATAAC TCATCTTTGA TGTGGTATAA 1200 ATGTATAATA ACTATATTAC ACTGGTATTT TATTTCAGTT ATATACTATA TAGTATTAAA 1260 AATTATATTT GTATAATTAT ATTATTATAT TCAGTGTAGA AAGTAAAATA CTATAAATAT 1320 GTATCTCTTA TTTATAACTT ATTAGTAAAG TATGTACTAT TCAGTTATAT TGTTTTATAA 1380 AAGCTAAATG CTACTAGATT GATATAAATG AATATGTAAT AAATTAGTAA TGTAGTATAC 1440 TAATATTAAC TCACATTATG AATACTACTA ATCACGAAGA ATGCAGTAAA ACATATGATA 1500 CAAACATGTT AACAGTTTTA AAAGCCATTA GTAATAAACA GTACAATATA ATTAAGTCTT 1560 TACTTAAAAA AGATATTAAT GTTAATAGAT TATTAACTAG TTATTCTAAC GAAATATATA 1620 AACATTTAGA CATTACATTA TGTAATATAC TTATAGAACG TGCAGCAGAC ATAAACATTA 1680 TAGATAAGAA CAATCGTACA CCGTTGTTTT ATGCGGTAAA GAATAATGAT TATGATATGG 1740 TTAAACTCCT ATTAAAAAAT GGCGCGAATG TAAATTTACA AGATAGTATA GGATATTCAT 1800 GTCTTCACAT CGCAGGTATA CATAATAGTA ACATAGAAAT AGTAGATGCA TTGATATCAT 1860 ACAAACCAGA TTTAAACTCC CGCGATTGGG TAGGTAGAAC ACCGCTACAT ATCTTCGTGA 1920 TAGAATCTAA CTTTGAAGCT GTGAAATTAT TATTAAAGTC AGGTGCATAT GTAGGTTTGA 1980 AAGACAAATG TAAGCATTTT CCTATACACC ATTCTGTAAT GAAATTAGAT CACTTAATAT 2040 CAGGATTGTT ATTAAAATAT GGAGCAAATC CAAATACAAT TAACGGCAAT GGAAAAACAT 2100 TATTAAGCAT TGCTGTAACA TCTAATAATA CACTACTGGT AGAACAGCTG CTGTTATATG 2160 GAGCAGAAGT TAATAATGGT GGTTATGATG TTCCAGCTCC TATTATATCC GCTGTCAGTG 2220 TTAACAATTA TGATATTGTT AAGATACTGA TACATAATGG TGCGAATATA AATGTATCCA 2280 CGGAAGATGG TAGAACGTCT TTACATACAG CTATGTTTTG GAATAACGCT AAAATAATAG 2340 ATGAGTTGCT TAACTATGGA AGTGACATAA ACAGCGTAGA TACTTATGGT AGAACTCCGT 2400 TATCTTGTTA TCGTAGCTTA AGTTATGATA TCGCTACTAA ACTAATATCA CGTATCATTA 2460 TAACAGATGT CTATCGTGAA GCACCAGTAA ATATCAGCGG ATTTATAATT AATTTAAAAA 2520 CTATAGAAAA TAATGATATA TTCAAATTAA TTAAAGATGA TTGTATTAAA GAGATAAACA 2580 TACTTAAAAG TATAACCCTT AATAAATTTC ATTCATCTGA CATATTTATA CGATATAATA 2640 CTGATATATG TTTATTAACG AGATTTATTC AACATCCAAA GATAATAGAA CTAGACAAAA 2700 AACTCTACGC TTATAAATCT ATAGTCAACG AGAGAAAAAT CAAAGCTACT TACAGGTATT 2760 ATCAAATAAA AAAAGTATTA ACTGTACTAC CTTTTTCAGG ATATTTCTCT ATATTGCCGT 2820 TTGATGTGTT AGTATATATA CTTGAATTCA TCTATGATAA TAATATGTTG GTACTTATGA 2880 GAGCGTTATC ATTAAAATGA AATAAAAAGC ATACAAGCTA TTGCTTCGCT ATCGTTACAA 2940 AATGGCAGGA ATTTTGTGTA AACTAAGCCA CATACTTGCC AATGAAAAAA ATAGTAGAAA 3000 GGATACTATT TTAATGGGAT TAGATGTTAA GGTTCCTTGG GATTATAGTA ACTGGGCATC 3060 TGTTAACTTT TACGACGTTA GGTTAGATAC TGATGTTACA GATTATAATA ATGTTACAAT 3120 AAAATACATG ACAGGATGTG ATATTTTTCC TCATATAACT CTTGGAATAG CAAATATGGA 3180 TCAATGTGAT AGATTTGAAA ATTTCAAAAA GCAAATAACT GATCAAGATT TACAGACTAT 3240 TTCTATAGTC TGTAAAGAAG AGATGTGTTT TCCTCAGAGT AACGCCTCTA AACAGTTGGG 3300 AGCGAAAGGA TGCGCTGTAG TTATGAAACT GGAGGTATCT GATGAACTTA GAGCCCTAAG 3360 AAATGTTCTG CTGAATGCGG TACCCTGTTC GAAGGACGTG TTTGGTGATA TCACAGTAGA 3420 TAATCCGTGG AATCCTCACA TAACAGTAGG ATATGTTAAG GAGGACGATG TCGAAAACAA 3480 GAAACGCCTA ATGGAGTGCA TGTCCAAGTT TAGGGGGCAA GAAATACAAG TTCTAGGATG 3540 GTATTAATAA GTATCTAAGT ATTTGGTATA ATTTATTAAA TAGTATAATT ATAACAAATA 3600 ATAAATAACA TGATAACGGT TTTTATTAGA ATAAAATAGA GATAATATCA TAATGATATA 3660 TAATACTTCA TTACCAGAAA TGAGTAATGG AAGACTTATA AATGAACTGC ATAAAGCTAT 3720 AAGGTATAGA GATATAAATT TAGTAAGGTA TATACTTAAA AAATGCAAAT ACAATAACGT 3780 AAATATACTA TCAACGTCTT TGTATTTAGC CGTAAGTATT TCTGATATAG AAATGGTAAA 3840 ATTATTACTA GAACACGGTG CCGATATTTT AAAATGTAAA AATCCTCCTC TTCATAAAGC 3900 TGCTAGTTTA GATAATACAG AAATTGCTAA ACTACTAATA GATTCTGGCG CTGACATAGA 3960 ACAGATACAT TCTGGAAATA GTCCGTTATA TATTTCTGTA TATAGAAACA ATAAGTCATT 4020 AACTAGATAT TTATTAAAAA AAGGTGTTAA TTGTAATAGA TTCTTTCTAA ATTATTACGA 4080 TGTACTGTAT GATAAGATAT CTGATGATAT GTATAAAATA TTTATAGATT TTAATATTGA 4140 TCTTAATATA CAAACTAGAA ATTTTGAAAC TCCGTTACAT TACGCTATAA AGTATAAGAA 4200 TATAGATTTA ATTAGGATAT TGTTAGATAA TAGTATTAAA ATAGATAAAA GTTTATTTTT 4260 GCATAAACAG TATCTCATAA AGGCACTTAA AAATAATTGT AGTTACGATA TAATAGCGTT 4320 ACTTATAAAT CACGGAGTGC CTATAAACGA ACAAGATGAT TTAGGTAAAA CCCCATTACA 4380 TCATTCGGTA ATTAATAGAA GAAAAGATGT AACAGCACTT CTGTTAAATC TAGGAGCTGA 4440 TATAAACGTA ATAGATGACT GTATGGGCAG TCCCTTACAT TACGCTGTTT CACGTAACGA 4500 TATCGAAACA ACAAAGACAC TTTTAGAAAG AGGATCTAAT GTTAATGTGG TTAATAATCA 4560 TATAGATACC GTTCTAAATA TAGCTGTTGC ATCTAAAAAC AAAACTATAG TAAACTTATT 4620 ACTGAAGTAC GGTACTGATA CAAAGTTGGT AGGATTAGAT AAACATGTTA TTCACATAGC 4680 TATAGAAATG AAAGATATTA ATATACTGAA TGCGATCTTA TTATATGGTT GCTATGTAAA 4740 CGTCTATAAT CATAAAGGTT TCACTCCTCT ATACATGGCA GTTAGTTCTA TGAAAACAGA 4800 ATTTGTTAAA CTCTTACTTG ACCACGGTGC TTACGTAAAT GCTAAAGCTA AGTTATCTGG 4860 AAATACTCCT TTACATAAAG CTATGTTATC TAATAGTTTT AATAATATAA AATTACTTTT 4920 ATCTTATAAC GCCGACTATA ATTCTCTAAA TAATCACGGT AATACGCCTC TAACTTGTGT 4980 TAGCTTTTTA GATGACAAGA TAGCTATTAT GATAATATCT AAAATGATGT TAGAAATATC 5040 TAAAAATCCT GAAATAGCTA ATTCAGAAGG TTTTATAGTA AACATGGAAC ATATAAACAG 5100 TAATAAAAGA CTACTATCTA TAAAAGAATC ATGCGAAAAA GAACTAGATG TTATAACACA 5160 TATAAAGTTA AATTCTATAT ATTCTTTTAA TATCTTTCTT GACAATAACA TAGATCTTAT 5220 GGTAAAGTTC GTAACTAATC CTAGAGTTAA TAAGATACCT GCATGTATAC GTATATATAG 5280 GGAATTAATA CGGAAAAATA AATCATTAGC TTTTCATAGA CATCAGCTAA TAGTTAAAGC 5340 TGTAAAAGAG AGTAAGAATC TAGGAATAAT AGGTAGGTTA CCTATAGATA TCAAACATAT 5400 AATAATGGAA CTATTAAGTA ATAATGATTT ACATTCTGTT ATCACCAGCT GTTGTAACCC 5460 AGTAGTATAA AGTGATTTTA TTCAATTACG AAGATAAACA TTAAATTTGT TAACAGATAT 5520 GAGTTATGAG TATTTAACTA AAGTTACTTT AGGTACAAAT AAAATATTAT GTAATATAAT 5580 AGAAAATTAT CTTGAGTCTT CATTTCCATC ACCGTCTAAA TTTATTATTA AAACCTTATT 5640 ATATAAGGCT GTTGAGTTTA GAAATGTAAA TGCTGTAAAA AAAATATTAC AGAATGATAT 5700 TGAATATGTT AAAGTAGATA GTCATGGTGT CTCGCCTTTA CATATTATAG CTATGCCTTC 5760 AAATTTTTCT CTCATAGACG CTGACATGTA TTCAGAATTT AATGAAATTA GTAATAGACT 5820 TCAAAAATCT AAAGATAGTA ACGAATTTCA ACGAGTTAGT CTACTAAGGA CAATTATAGA 5880 ATATGGTAAT GATAGTGATA TTAATAAGTG TCTAACATTA GTAAAAACGG ATATACAGAG 5940 TAACGAAGAG ATAGATATTA TAGATCTTTT GATAAATAAA GGAATAGATA TAAATATTAA 6000 AGACGATTTA GGAAACACAG CTTTGCATTA CTCGTGTGAT TATGCTAAGG GATCAAAGAT 6060 AGCTAAAAAG TTACTAGATT GTGGAGCAGA TCCTAACATA GTTAATGATT TAGGTGTTAC 6120 ACCACTAGCG TGTGCCGTTA ATACTTGCAA CGAGATACTA GTAGATATTC TGTTAAATAA 6180 TGATGCGAAT CCTGATTCAT CTTCCTCATA TTTTTTAGGT ACTAATGTGT TACATACAGC 6240 CGTAGGTACC GGTAATATAG ATATTGTAAG ATCTTTACTT ACGGCTGGTG CCAATCCTAA 6300 TGTAGGAGAT AAATCTGGAG TTACTCCTTT GCACGTTGCT GCAGCTGATA AAGACAGTTA 6360 TCTGTTAATG GAGATGCTAC TAGATAGCGG GGCAGATCCA AATATAAAAT GCGCAAACGG 6420 TTTTACTCCT TTGTTTAATG CAGTATATGA TCATAACCGT ATAAAGTTAT TATTTCTTTA 6480 CGGGGCTGAT ATCAATATTA CTGACTCTTA CGGAAATACT CCTCTTACTT ATATGACTAA 6540 TTTTGATAAT AAATATGTAA ATTCAATAAT TATCTTACAA ATATATCTAC TTAAAAAAGA 6600 ATATAACGAT GAAAGATTGT TTCCACCTGG TATGATAAAA AATTTAAACT TTATAGAATC 6660 AAACGATAGT CTTAAAGTTA TAGCTAAAAA GTGTAATTCG TTAATACGCT ATAAGAAAAA 6720 TAAAGACATA GATGCAGATA ACGTATTATT GGAGCTTTTA GAGGAAGAGG AAGAAGATGA 6780 AATAGACAGA TGGCATACTA CATGTAAAAT ATCTTAAATA GTAATTAAAT CATTGAAATA 6840 TTAACTTACA AGATGATCGA GGTCACTTAT TATACTCTTT AATAATGGGT ACAAAGAGTA 6900 TTCATACGTT AGTTAAATCT AACGATGTAA TACGTGTTCG TGAATTAATA AAGGATGATA 6960 GATGTTTGAT AAATAAAAGA AATAGAAGAA ATCAGTCACC TGTATATATA GCTATATACA 7020 AAGGACTTTA TGAAATGACT GAAATGTTAT TGCTAAATAA TGCAAGTCTA GATACTAAAA 7080 TACCTTCTTT AATTATAGCA GCTAAAAATA ATGACTTACC TATGATAAAA TTATTGATAC 7140 AATACGGGGC AAAATTAAAT GATATTTATT TAAGGGACAC AGCATTAATG ATAGCTCTCA 7200 GAAATGGTTA CCTAGATATA GCTGAATATT TACTTTCATT AGGAGCAGAA TTTGTTAAAT 7260 ACAGACATAA GGTAATATAT AAATATCTAT CAAAAGATGC GTATGAATTA CTTTTTAGAT 7320 TTAATTATGA CGTTAATATA ATAGATTGAG A 7351 7091 base pairs nucleic acid single linear DNA (genomic) unknown 4 AGATATTTGT TAGCTTCTGC CGGAGATACC GTGAAAATCT ATTTTCTGGA AGGAAAGGGA 60 GGTCTTATCT ATTCTGTCAG CAGAGTAGGT TCCTCTAATG ACGAAGACAA TAGTGAATAC 120 TTGCATGAAG GTCACTGTGT AGAGTTCAAA ACTGATCATC AGTGTTTGAT AACTCTAGCG 180 TGTACGAGTC CTTCTAACAC TGTGGTTTAT TGGCTGGAAT AAAAGGATAA AGACACCTAT 240 ACTGATTCAT TTTCATCTGT CAACGTTTCT CTAAGAGATT CATAGGTATT ATTATTACAT 300 CGATCTAGAA GTCTAATAAC TGCTAAGTAT ATTATTGGAT TTAACGCGCT ATAAACGCAT 360 CCAAAACCTA CAAATATAGG AGAAGCTTCT CTTATGAAAC TTCTTAAAGC TTTACTCTTA 420 CTATTACTAC TCAAAAGAGA TATTACATTA ATTATGTGAT GAGGCATCCA ACATATAAAG 480 AAGACTAAAG CTGTAGAAGC TGTTATGAAG AATATCTTAT CAGATATATT AGATGCATTG 540 TTAGTTCTGT AGATCAGTAA CGTATAGCAT ACGAGTATAA TTATCGTAGG TAGTAGGTAT 600 CCTAAAATAA ATCTGATACA GATAATAACT TTGTAAATCA ATTCAGCAAT TTCTCTATTA 660 TCATGATAAT GATTAATACA CAGCGTGTCG TTATTTTTTG TTACGATAGT ATTTCTAAAG 720 TAAAGAGCAG GAATCCCTAG TATAATAGAA ATAATCCATA TGAAAAATAT AGTAATGTAC 780 ATATTTCTAA TGTTAACATA TTTATAGGTA AATCCAGGAA GGGTAATTTT TACATATCTA 840 TATACGCTTA TTACAGTTAT TAAAAATATA CTTGCAAACA TGTTAGAAGT AAAAAAGAAA 900 GAACTAATTT TACAAAGTGC TTTACCAAAA TGCCAATGGA AATTACTTAG TATGTATATA 960 ATGTATAAAG GTATGAATAT CACAAACAGC AAATCGGCTA TTCCCAAGTT GAGAAACGGT 1020 ATAATAGATA TATTTCTAGA TACCATTAAT AACCTTATAA GCTTGACGTT TCCTATAATG 1080 CCTACTAAGA AAACTAGAAG ATACATACAT ACTAACGCCA TACGAGAGTA ACTACTCATC 1140 GTATAACTAC TGTTGCTAAC AGTGACACTG ATGTTATAAC TCATCTTTGA TGTGGTATAA 1200 ATGTATAATA ACTATATTAC ACTGGTATTT TATTTCAGTT ATATACTATA TAGTATTAAA 1260 AATTATATTT GTATAATTAT ATTATTATAT TCAGTGTAGA AAGTAAAATA CTATAAATAT 1320 GTATCTCTTA TTTATAACTT ATTAGTAAAG TATGTACTAT TCAGTTATAT TGTTTTATAA 1380 AAGCTAAATG CTACTAGATT GATATAAATG AATATGTAAT AAATTAGTAA TGTAGTATAC 1440 TAATATTAAC TCACATTTGA CTAATTAGCT ATAAAAACCC GGGCTGCAGG AATTCCTCGA 1500 GACGCGTGGC ATGCAAGCTT ATAAAAATCA CAAGTCTCTG TCACTTTTTT TGTCTAGTTT 1560 TTTTTTCTCC TCTTGGTTCA GACGTTCTCT TCTTCGTCGG AGTCTTTCAA GTGTCGGTAG 1620 CCGTTTTTGC GGTGTCGCAG TCGGTCTAGC AGGTTGGGCT TCTGTCCCTT GTCCTGCGTG 1680 CCAGTCTGTC CGTCCAAAGA ATCTGTACCG TTCTCGTGCG CTCGCTGCTC TGCGTCCAGA 1740 CGGACCAGGG CCAGAAGCAT CTGGTAAGCC TGCTCGTTGG TGTAAGGCGG AGCCGCCGTG 1800 GATGCATCAG ACGACGGTGG TCCCGGTCCT TTGCGACCAG AATTATAAAC ACTTTCCTCG 1860 TAGGAAGGCG GAGCCTGTAA CGACGTGTCT TTGGTGTTGC CCGACGTCAC GGTGGTCCCG 1920 TCGGCGGACA CCAGATAGGG AAAGAGGTTC TGCAGCGGCT GCATGCAGAG ACGCCGCTGT 1980 CGAGTATAGA TCAAATAAAT GATAATGACG ACGGCTATGG CCACGAGGAT GATGGTGAAG 2040 GCTCCGAAGG GGTTTTTGAG GAAGGTGGCA ACGCCTTCGA CCACGGAGGC CACCGCGCCA 2100 CCCACGGCCC CAATGGCTAC GCCAACGGCC TTTCCCGCGG CGCCCAGGCC GCTCATGAGG 2160 TCGTCCAGAC CCTTGAGGTA GGGCGGCAGC GGGTCGACTA CCTTGTCCTC CACGTACTTT 2220 ACCCGCTGCT TATACGAATT GAACTCGCGC ATGATCTCCT CGAGATCAAA AACGTTGCTG 2280 GAACGCAATT CTTTCTGCGA GTAAAGTTCC AGTACCCTGA AGTCGGTGTT TTCCAGCGGG 2340 TCGATGTCTA GGGCGATCAT GCTGTCGACG GTGGAGATGC TGCTGAGGTC AATCATGCGT 2400 TTGAAGAGGT AGTCCACGTA CTCGTAGGCC GAGTTGCCGG CGATGAAGAT CTTGAGGCTG 2460 GGAAGCTGAC ATTCCTCAGT GCGGTGGTTG CCCAACAGGA TTTCGTTATC CTCGCCCAGT 2520 TGACCGTACT GCACGTACGA GCTGTTGGCG AAATTAAAGA TGACCACTGG TCGTGAGTAG 2580 CAGCGTCCTG GCGATTCCTT CACATTCATA TCACGCAGCA CCTTGACGCT GGTTTGGTTA 2640 ATGGTCACGC AGCTGGCCAG ACCCAGGACA TCACCCATGA AACGCGCGGC AATCGGTTTG 2700 TTGTAGATGG CCGAGAGAAT AGCTGACGGG TTGATCTTGC TAAGTTCCTT GAAGACCTCT 2760 AGGGTGCGCC GTTGATCCAC ACACCAGGCT TCTGCGATTT CGGCCAGCGC CCGGTTGATG 2820 TAACCGCGCA ACGTGTCATA GGTGAACTGC AGCTGGGCGT AGACCAGATT GTGCACCGAC 2880 TCCATGTTGG ATAAATGAGT TGCATTGTTG CCATCTGTAC TTCTTTTGGT TCTATTATGA 2940 GTAAGATTCA GACTGGAGCG GTTGGCCAAA CGTTCGAGTT CCACCAGAGA TTTTTGCTTG 3000 ATACCTTGCC AGAACACCAC CAAACCACCA GTGGTTTCAA AGACCGACAC GTTTCCATAT 3060 TTTTCATATG TTTGATTGTA TGAAGTATTG AAAATCTGCT GTAACTTATT TATGGCCTCA 3120 TCACGTACAC AGTCCAGCGC AGAGTCGGAC ATGTTCACCT CTTGCTTCTT AGATAAGAAA 3180 GTGGCGGTCA TTTTGGCAGA AGAAAAGTGA TACGAGTCCT CGGCTTCGGA ACGAATGGTG 3240 CGTTCCGAGG CTTCCCAGAA AGTGAGTTGA CAAGTAACAT TCTTCTCGTC CTGTATATCC 3300 CAGGAGATCA CTGAGTCCGC ACGTTCAAGA AAAGCCACCA ACCTGTGGGT CTCTAACGCA 3360 GAATTCGGTC TTTCAAAGTC GGAGACGATA GTGTAGTTCG GAAAAATGAA AAACTTGTCG 3420 GCGTTTTCTC CAAAATAGCT GGCATTGCGA TTAGTTCCGT TGTAGAAAGG AGAAATGTCA 3480 ACCACATCAC CCGTGGAAGT TGCGAAAAAA TGATAGGGAT ACTTGGAGCG CGCAGTAGTG 3540 ATGGTCACCA TACAATTCAG ATTACAGGTC TCACGATAGA GCCAGGTGCT GCCGCGGCTG 3600 TGCCATTGAT CCTTGACCGT CACGTAACGG GTACTGTGGG TGTTGGAATA ATCGTCGGGC 3660 ATTAATTGCA TGGTTTTGTT TTCATAGCTG TCCCTATGAT AAGCCACGAA AACCGTGCCT 3720 GCTATAACGC GGCTGTAGGA ACTGTAGCAC TGACTGTGAC TGTTGATATG ATGAATCTCC 3780 CACATAGGAG GCGCCACGTA TTCCGTGTTG CTGCCCAGCA GATAAGTGGT GTGGATGTAA 3840 GCGTAGCTAC GACGAAACGT CAAAACCTTC TGGTAGACTC GTACCTTAAA GGTGTGCGCG 3900 ACGATGTTGC GTTTGTAGAC CACCATGATG CCCTCGTCCA GGTCTTCATT GATGGGCTTC 3960 ATCGAGGTGC AGACGATATT ACGTTCAAAG CGAATAAGAT CCGTACCCTG AGCCATAGAA 4020 CACACGCGAT AGGGGTACTT GGTGGTGTTG ACCCCCACCA CATCTCCGTA CTTGAGGGTA 4080 GTGTTGTAGA TGGTCTCGTT AACACCATGG CTGACCGTTT GGGAAGAAGT TACGCGTTGA 4140 GAGACTGAAC CGGATCGAGA ATGAGCAGCA GACGTCGTAT GAGAGGAATG GTGACTGTGA 4200 GTAGCAGAAG TTCCACGAGT AGAAGATGAG GAAACCGCAG CACCCAGACA GACGATACAC 4260 AAGTTAACGC AGACTACCAG GCACCAGATC CTGGATTCCA TTACGATACA AACTTAACGG 4320 ATATCGCGAT AATGAAATAA TTTATGATTA TTTCTCGCTT TCAATTTAAC ACAACCCTCA 4380 AGAACCTTTG TATTTATTTT CACTTTTTAA GTATAGAATA AAGAAGCTCT AATTAATTAA 4440 GCTACAAATA GTTTCGTTTT CACCTTGTCT AATAACTAAT TAATTAACCC GGATCCCGAT 4500 TTTTATGACT AGTTAATCAA ATAAAAAGCA TACAAGCTAT TGCTTCGCTA TCGTTACAAA 4560 ATGGCAGGAA TTTTGTGTAA ACTAAGCCAC ATACTTGCCA ATGAAAAAAA TAGTAGAAAG 4620 GATACTATTT TAATGGGATT AGATGTTAAG GTTCCTTGGG ATTATAGTAA CTGGGCATCT 4680 GTTAACTTTT ACGACGTTAG GTTAGATACT GATGTTACAG ATTATAATAA TGTTACAATA 4740 AAATACATGA CAGGATGTGA TATTTTTCCT CATATAACTC TTGGAATAGC AAATATGGAT 4800 CAATGTGATA GATTTGAAAA TTTCAAAAAG CAAATAACTG ATCAAGATTT ACAGACTATT 4860 TCTATAGTCT GTAAAGAAGA GATGTGTTTT CCTCAGAGTA ACGCCTCTAA ACAGTTGGGA 4920 GCGAAAGGAT GCGCTGTAGT TATGAAACTG GAGGTATCTG ATGAACTTAG AGCCCTAAGA 4980 AATGTTCTGC TGAATGCGGT ACCCTGTTCG AAGGACGTGT TTGGTGATAT CACAGTAGAT 5040 AATCCGTGGA ATCCTCACAT AACAGTAGGA TATGTTAAGG AGGACGATGT CGAAAACAAG 5100 AAACGCCTAA TGGAGTGCAT GTCCAAGTTT AGGGGGCAAG AAATACAAGT TCTAGGATGG 5160 TATTAATAAG TATCTAAGTA TTTGGTATAA TTTATTAAAT AGTATAATTA TAACAAATAA 5220 TAAATAACAT GATAACGGTT TTTATTAGAA TAAAATAGAG ATAATATCAT AATGATATAT 5280 AATACTTCAT TACCAGAAAT GAGTAATGGA AGACTTATAA ATGAACTGCA TAAAGCTATA 5340 AGGTATAGAG ATATAAATTT AGTAAGGTAT ATACTTAAAA AATGCAAATA CAATAACGTA 5400 AATATACTAT CAACGTCTTT GTATTTAGCC GTAAGTATTT CTGATATAGA AATGGTAAAA 5460 TTATTACTAG AACACGGTGC CGATATTTTA AAATGTAAAA ATCCTCCTCT TCATAAAGCT 5520 GCTAGTTTAG ATAATACAGA AATTGCTAAA CTACTAATAG ATTCTGGCGC TGACATAGAA 5580 CAGATACATT CTGGAAATAG TCCGTTATAT ATTTCTGTAT ATAGAAACAA TAAGTCATTA 5640 ACTAGATATT TATTAAAAAA AGGTGTTAAT TGTAATAGAT TCTTTCTAAA TTATTACGAT 5700 GTACTGTATG ATAAGATATC TGATGATATG TATAAAATAT TTATAGATTT TAATATTGAT 5760 CTTAATATAC AAACTAGAAA TTTTGAAACT CCGTTACATT ACGCTATAAA GTATAAGAAT 5820 ATAGATTTAA TTAGGATATT GTTAGATAAT AGTATTAAAA TAGATAAAAG TTTATTTTTG 5880 CATAAACAGT ATCTCATAAA GGCACTTAAA AATAATTGTA GTTACGATAT AATAGCGTTA 5940 CTTATAAATC ACGGAGTGCC TATAAACGAA CAAGATGATT TAGGTAAAAC CCCATTACAT 6000 CATTCGGTAA TTAATAGAAG AAAAGATGTA ACAGCACTTC TGTTAAATCT AGGAGCTGAT 6060 ATAAACGTAA TAGATGACTG TATGGGCAGT CCCTTACATT ACGCTGTTTC ACGTAACGAT 6120 ATCGAAACAA CAAAGACACT TTTAGAAAGA GGATCTAATG TTAATGTGGT TAATAATCAT 6180 ATAGATACCG TTCTAAATAT AGCTGTTGCA TCTAAAAACA AAACTATAGT AAACTTATTA 6240 CTGAAGTACG GTACTGATAC AAAGTTGGTA GGATTAGATA AACATGTTAT TCACATAGCT 6300 ATAGAAATGA AAGATATTAA TATACTGAAT GCGATCTTAT TATATGGTTG CTATGTAAAC 6360 GTCTATAATC ATAAAGGTTT CACTCCTCTA TACATGGCAG TTAGTTCTAT GAAAACAGAA 6420 TTTGTTAAAC TCTTACTTGA CCACGGTGCT TACGTAAATG CTAAAGCTAA GTTATCTGGA 6480 AATACTCCTT TACATAAAGC TATGTTATCT AATAGTTTTA ATAATATAAA ATTACTTTTA 6540 TCTTATAACG CCGACTATAA TTCTCTAAAT AATCACGGTA ATACGCCTCT AACTTGTGTT 6600 AGCTTTTTAG ATGACAAGAT AGCTATTATG ATAATATCTA AAATGATGTT AGAAATATCT 6660 AAAAATCCTG AAATAGCTAA TTCAGAAGGT TTTATAGTAA ACATGGAACA TATAAACAGT 6720 AATAAAAGAC TACTATCTAT AAAAGAATCA TGCGAAAAAG AACTAGATGT TATAACACAT 6780 ATAAAGTTAA ATTCTATATA TTCTTTTAAT ATCTTTCTTG ACAATAACAT AGATCTTATG 6840 GTAAAGTTCG TAACTAATCC TAGAGTTAAT AAGATACCTG CATGTATACG TATATATAGG 6900 GAATTAATAC GGAAAAATAA ATCATTAGCT TTTCATAGAC ATCAGCTAAT AGTTAAAGCT 6960 GTAAAAGAGA GTAAGAATCT AGGAATAATA GGTAGGTTAC CTATAGATAT CAAACATATA 7020 ATAATGGAAC TATTAAGTAA TAATGATTTA CATTCTGTTA TCACCAGCTG TTGTAACCCA 7080 GTAGTATAAA G 7091 4768 base pairs nucleic acid single linear DNA (genomic) unknown 5 AAGCTTGCGG CCGCTCATTA GACAAGCGAA TGAGGGACGA AAACGTGGAG GAGGTATTAA 60 GTTTGGAGAA ATGGAGAGAG ACTGTTTAAT AGCGCATGGC GCAGCCAATA CTATTACAGA 120 AGTTTTGAAA GATTCGGAAG AAGATTATCA AGATGTGTAT GTTTGTGAAA ATTGTGGAGA 180 CATAGCAGCA CAAATCAAGG GTATTAATAC ATGTCTTAGA TGTTCAAAAC TTAATCTCTC 240 TCCTCTCTTA ACAAAAATTG ATACCACGCA CGTATCTAAA GTATTTCTTA CTCAAATGAA 300 CGCCAGAGGC GTAAAAGTCA AATTAGATTT CGAACGAAGG CCTCCTTCGT TTTATAAACC 360 ATTAGATAAA GTTGATCTCA AGCCGTCTTT TCTGGTGTAA TAAAAATTAA TTAATTACTC 420 GAGGGTACCG GATCCCCCAG CTTATAAAAA TCACAAGTCT CTGACACTTT TTTTGTCTAG 480 TTTTTTTTTC TCCTCTTGGT TCAGACGTTC TCTTCTTCGT CGGAGTCTTT CAAGTGTCGG 540 TAGCCGTTTT TGCGGTGTCG CAGTCGGTCT AGCAGGTTGG GCTTCTGTCC CTTGTCCTGC 600 GTGCCAGTCT GTCCGTCCAA AGAATCTGTA CCGTTCTCGT GCGCTCGCTG CTCTGCGTCC 660 AGACGGACCA GGGCCAGAAG CATCTGGTAA GCCTGCTCGT TGGTGTAAGG CGGAGCCGCC 720 GTGGATGCAT CAGACGACGG TGGTCCCGGT CCTTTGCGAC CAGAATTATA AACACTTTCC 780 TCGTAGGAAG GCGGAGCCTG TAACGACGTG TCTTTGGTGT TGCCCGACGT CACGGTGGTC 840 CCGTCGGCGG ACACCAGATA GGGAAAGAGG TTCTGCAGCG GCTGCATGCA GAGACGCCGC 900 TGTCGAGTAT AGATCAAATA AATGATAATG ACGACGGCTA TGGCCACGAG GATGATGGTG 960 AAGGCTCCGA AGGGGTTTTT GAGGAAGGTG GCAACGCCTT CGACCACGGA GGCCACCGCG 1020 CCACCCACGG CCCCAATGGC TACGCCAACG GCCTTTCCCG CGGCGCCCAG GCCGCTCATG 1080 AGGTCGTCCA GACCCTTGAG GTAGGGCGGC AGCGGGTCGA CTACCTTGTC CTCCACGTAC 1140 TTTACCCGCT GCTTATACGA ATTGAACTCG CGCATGATCT CCTCGAGATC AAAAACGTTG 1200 CTGGAACGCA ATTCTTTCTG CGAGTAAAGT TCCAGTACCC TGAAGTCGGT GTTTTCCAGC 1260 GGGTCGATGT CTAGGGCGAT CATGCTGTCG ACGGTGGAGA TGCTGCTGAG GTCAATCATG 1320 CGTTTGAAGA GGTAGTCCAC GTACTCGTAG GCCGAGTTGC CGGCGATGAA GATCTTGAGG 1380 CTGGGAAGCT GACATTCCTC AGTGCGGTGG TTGCCCAACA GGATTTCGTT ATCCTCGCCC 1440 AGTTGACCGT ACTGCACGTA CGAGCTGTTG GCGAAATTAA AGATGACCAC TGGTCGTGAG 1500 TAGCAGCGTC CTGGCGATTC CTTCACATTC ATATCACGCA GCACCTTGAC GCTGGTTTGG 1560 TTAATGGTCA CGCAGCTGGC CAGACCCAGG ACATCACCCA TGAAACGCGC GGCAATCGGT 1620 TTGTTGTAGA TGGCCGAGAG AATAGCTGAC GGGTTGATCT TGCTAAGTTC CTTGAAGACC 1680 TCTAGGGTGC GCCGTTGATC CACACACCAG GCTTCTGCGA TTTCGGCCAG CGCCCGGTTG 1740 ATGTAACCGC GCAACGTGTC ATAGGTGAAC TGCAGCTGGG CGTAGACCAG ATTGTGCACC 1800 GACTCCATGT TGGATAAATG AGTTGCATTG TTGCCATCTG TACTTCTTTT GGTTCTATTA 1860 TGAGTAAGAT TCAGACTGGA GCGGTTGGCC AAACGTTCGA GTTCCACCAG AGATTTTTGC 1920 TTGATACCTT GCCAGAACAC CACCAAACCA CCAGTGGTTT CAAAGACGGA CACGTTTCCA 1980 TATTTTTCAT ATGTTTGATT GTATGAAGTA TTGAAAATCT GCTGTAACTT ATTTATGGCC 2040 TCATCACGTA CACAGTCCAG CGCAGAGTCG GACATGTTCA CCTCTTGCTT CTTAGATAAG 2100 AAAGTGGCGG TCATTTTGGC AGAAGAAAAG TGATACGAGT CCTCGGCTTC GGAACGAATG 2160 GTGCGTTCCG AGGCTTCCCA GAAAGTGAGT TGACAAGTAA CATTCTTCTC GTCCTGTATA 2220 TCCCAGGAGA TCACTGAGTC CGCACGTTCA AGAAAAGCCA CCAACCTGTG GGTCTCTAAC 2280 GCAGAATTCG GTCTTTCAAA GTCGGAGACG ATAGTGTAGT TCGGAAAAAT GAAAAACTTG 2340 TCGGCGTTTT CTCCAAAATA GCTGGCATTG CGATTAGTTC CGTTGTAGAA AGGAGAAATG 2400 TCAACCACAT CACCCGTGGA AGTTGCGAAA AAATGATAGG GATACTTGGA GCGCGCAGTA 2460 GTGATGGTCA CCATACAATT CAGATTACAG GTCTCACGAT AGAGCCAGGT GCTGCCGCGG 2520 CTGTGCCATT GATCCTTGAC CGTCACGTAA CGGGTACTGT GGGTGTTGGA ATAATCGTCG 2580 GGCATTAATT GCATGGTTTT GTTTTCATAG CTGTCCCTAT GATAAGCCAC GAAAACCGTG 2640 CCTGCTATAA CGCGGCTGTA GGAACTGTAG CACTGACTGT GACTGTTGAT ATGATGAATC 2700 TCCCACATAG GAGGCGCCAC GTATTCCGTG TTGCTGCCCA GCAGATAAGT GGTGTGGATG 2760 TAAGCGTAGC TACGACGAAA CGTCAAAACC TTCTGGTAGA CTCGTACCTT AAAGGTGTGC 2820 GCGACGATGT TGCGTTTGTA GACCACCATG ATGCCCTCGT CCAGGTCTTC ATTGATGGGC 2880 TTCATCGAGG TGCAGACGAT ATTACGTTCA AAGCGAATAA GATCCGTACC CTGAGCCATA 2940 GAACACACGC GATAGGGGTA CTTGGTGGTG TTGACCCCCA CCACATCTCC GTACTTGAGG 3000 GTAGTGTTGT AGATGGTCTC GTTAACACCA TGGCTGACCG TTTGGGAAGA AGTTACGCGT 3060 TGAGAGACTG AACCGGATCG AGAATGAGCA GCAGACGTCG TATGAGAGGA ATGGTGACTG 3120 TGAGTAGCAG AAGTTCCACG AGTAGAAGAT GAGGAAACCG CAGCACCCAG ACAGACGATA 3180 CACAAGTTAA CGCAGACTAC CAGGCACCAG ATCCTGGATT CCATTACGAT ACAAACTTAA 3240 CGGATATCGC GATAATGAAA TAATTTATGA TTATTTCTCG CTTTCAATTT AACACAACCC 3300 TCAAGAACCT TTGTATTTAT TTTCACTTTT TAAGTATAGA ATAAAGAAGC TGGGAATCGA 3360 TTCGCGATAG CTGATTAGTT TTTGTTAACA AAAATGTGGG AGAATCTAAT TAGTTTTTCT 3420 TTACACAATT GACGTACATG AGTCTGAGTT CCTTGTTTTT GCTAATTATT TCATCCAATT 3480 TATTATTCTT GACGATATCG AGATCTTTTG TATAGGAGTC AGACTTGTAT TCAACATGCT 3540 TTTCTATAAT CATCTTAGTT ATTTCGGCAT CATCCAATAG TACATTTTCC AGATTAACAG 3600 AGTAGATATT AATGTCGTAT TTGAACAGAG CCTGTAACAT CTCAATGTCT TTATTATCTA 3660 TAGCCAATTT AATGTCCGGA ATGAAGAGAA GGGAATTATT GGTGTTTGTC GACGTCATAT 3720 AGTCGAGCAA GAGAATCATC ATATCCACGT GTCCATTTTT TATAGTGGTG TGAATACAAC 3780 TAAGGAGAAT AGCCAGATCA AAAGTAGATG GTATTTCTGA AAGAAAGTAT GATACAATAC 3840 TTACATCATT AAGCATGACG GCATGATAAA ATGAAGTTTT CCATCCAGTT TTCCCATAGA 3900 ACATCAGTCT CCAATTTTTC TTAAACAGTT TCACCGTTTG CATGTTACCA CTATCAACCG 3960 CATAATACAA TGCGGTGTTT CCTTTGTCAT CAAATTGTGA ATCATCCATT CCACTGAATA 4020 GCAAAATCTT TACTATTTTG GTATCTTCTA ATGTGGCTGC CTGATGTAAT GGAAATTCAT 4080 TCTCTAGAAG ATTTTTCAAT GCTCCAGCGT TCAACAACGT ACATACTAGA CGCACGTTAT 4140 TATCAGCTAT TGCATAATAC AAGGCACTAT GTCCATGGAC ATCCGCCTTA AATGTATCTT 4200 TACTAGAGAG AAAGCTTTTC AGCTGCTTAG ACTTCCAAGT ATTAATTCGT GACAGATCCA 4260 TGTCTGAAAC GAGACGCTAA TTAGTGTATA TTTTTTCATT TTTTATAATT TTGTCATATT 4320 GCACCAGAAT TAATAATATC TCTAATAGAT CTAATTTAAT TTAATTTATA TAACTTATTT 4380 TTTGAATATA CTTTTAATTA ACAAAAGAGT TAAGTTACTC ATATGGACGC CGTCCAGTCT 4440 GAACATCAAT CTTTTTAGCC AGAGATATCA TAGCCGCTCT TAGAGTTTCA GCGTGATTTT 4500 CCAACCTAAA TAGAACTTCA TCGTTGCGTT TACAACACTT TTCTATTTGT TCAAACTTTG 4560 TTGTTACATT AGTAATCTTT TTTTCCAAAT TAGTTAGCCG TTGTTTGAGA GTTTCCTCAT 4620 TGTCGTCTTC ATCGGCTTTA ACAATTGCTT CGCGTTTAGC CTCCTGGCTG TTCTTATCAG 4680 CCTTTGTAGA AAAAAATTCA GTTGCTGGAA TTGCAAGATC GTCATCTCCG GGGAAAAGAG 4740 TTCCGTCCAT TTAAAGCCGC GGGAATTC 4768 2550 base pairs nucleic acid single linear DNA (genomic) unknown 6 ATGGAATCCA GGATCTGGTG CCTGGTAGTC TGCGTTAACT TGTGTATCGT CTGTCTGGGT 60 GCTGCGGTTT CCTCATCTTC TACTCGTGGA ACTTCTGCTA CTCACAGTCA CCATTCCTCT 120 CATACGACGT CTGCTGCTCA TTCTCGATCC GGTTCAGTCT CTCAACGCGT AACTTCTTCC 180 CAAACGGTCA GCCATGGTGT TAACGAGACC ATCTACAACA CTACCCTCAA GTACGGAGAT 240 GTGGTGGGGG TCAACACCAC CAAGTACCCC TATCGCGTGT GTTCTATGGC TCAGGGTACG 300 GATCTTATTC GCTTTGAACG TAATATCGTC TGCACCTCGA TGAAGCCCAT CAATGAAGAC 360 CTGGACGAGG GCATCATGGT GGTCTACAAA CGCAACATCG TCGCGCACAC CTTTAAGGTA 420 CGAGTCTACC AGAAGGTTTT GACGTTTCGT CGTAGCTACG CTTACATCCA CACCACTTAT 480 CTGCTGGGCA GCAACACGGA ATACGTGGCG CCTCCTATGT GGGAGATTCA TCATATCAAC 540 AGTCACAGTC AGTGCTACAG TTCCTACAGC CGCGTTATAG CAGGCACGGT TTTCGTGGCT 600 TATCATAGGG ACAGCTATGA AAACAAAACC ATGCAATTAA TGCCCGACGA TTATTCCAAC 660 ACCCACAGTA CCCGTTACGT GACGGTCAAG GATCAATGGC ACAGCCGCGG CAGCACCTGG 720 CTCTATCGTG AGACCTGTAA TCTGAATTGT ATGGTGACCA TCACTACTGC GCGCTCCAAG 780 TATCCCTATC ATTTTTTCGC AACTTCCACG GGTGATGTGG TTGACATTTC TCCTTTCTAC 840 AACGGAACTA ATCGCAATGC CAGCTATTTT GGAGAAAACG CCGACAAGTT TTTCATTTTT 900 CCGAACTACA CTATCGTCTC CGACTTTGAA AGACCGAATT CTGCGTTAGA GACCCACAGG 960 TTGGTGGCTT TTCTTGAACG TGCGGACTCA GTGATCTCCT GGGATATACA GGACGAGAAG 1020 AATGTTACTT GTCAACTCAC TTTCTGGGAA GCCTCGGAAC GCACCATTCG TTCCGAAGCC 1080 GAGGACTCGT ATCACTTTTC TTCTGCCAAA ATGACCGCCA CTTTCTTATC TAAGAAGCAA 1140 GAGGTGAACA TGTCCGACTC TGCGCTGGAC TGTGTACGTG ATGAGGCCAT AAATAAGTTA 1200 CAGCAGATTT TCAATACTTC ATACAATCAA ACATATGAAA AATATGGAAA CGTGTCCGTC 1260 TTTGAAACCA CTGGTGGTTT GGTGGTGTTC TGGCAAGGTA TCAAGCAAAA ATCTCTGGTG 1320 GAACTCGAAC GTTTGGCCAA CCGCTCCAGT CTGAATCTTA CTCATAATAG AACCAAAAGA 1380 AGTACAGATG GCAACAATGC AACTCATTTA TCCAACATGG AGTCGGTGCA CAATCTGGTC 1440 TACGCCCAGC TGCAGTTCAC CTATGACACG TTGCGCGGTT ACATCAACCG GGCGCTGGCC 1500 GAAATCGCAG AAGCCTGGTG TGTGGATCAA CGGCGCACCC TAGAGGTCTT CAAGGAACTT 1560 AGCAAGATCA ACCCGTCAGC TATTCTCTCG GCCATCTACA ACAAACCGAT TGCCGCGCGT 1620 TTCATGGGTG ATGTCCTGGG TCTGGCCAGC TGCGTGACCA TTAACCAAAC CAGCGTCAAG 1680 GTGCTGCGTG ATATGAATGT GAAGGAATCG CCAGGACGCT GCTACTCACG ACCAGTGGTC 1740 ATCTTTAATT TCGCCAACAG CTCGTACGTG CAGTACGGTC AACTGGGCGA GGATAACGAA 1800 ATCCTGTTGG GCAACCACCG CACTGAGGAA TGTCAGCTTC CCAGCCTCAA GATCTTCATC 1860 GCCGGCAACT CGGCCTACGA GTACGTGGAC TACCTCTTCA AACGCATGAT TGACCTCAGC 1920 AGCATCTCCA CCGTCGACAG CATGATCGCC CTAGACATCG ACCCGCTGGA AAACACCGAC 1980 TTCAGGGTAC TGGAACTTTA CTCGCAGAAA GAATTGCGTT CCAGCAACGT TTTTGATCTC 2040 GAGGAGATCA TGCGCGAGTT CAATTCGTAT AAGCAGCGGG TAAAGTACGT GGAGGACAAG 2100 GTAGTCGACC CGCTGCCGCC CTACCTCAAG GGTCTGGACG ACACTCGACA GCGGCGTCTC 2160 TGCATGCAGC CGCTGCAGAA CCTCTTTCCC TATCTGGTGT CCGCCGACGG GACCACCGTG 2220 ACGTCGGGCA ACACCAAAGA CACGTCGTTA CAGGCTCCGC CTTCCTACGA GGAAAGTGTT 2280 TATAATTCTG GTCGCAAAGG ACCGGGACCA CCGTCGTCTG ATGCATCCAC GGCGGCTCCG 2340 CCTTACACCA ACGAGCAGGC TTACCAGATG CTTCTGGCCC TGGTCCGTCT GGACGCAGAG 2400 CAGCGAGCGC ACGAGAACGG TACAGATTCT TTGGACGGAC AGACTGGCAC GCAGGACAAG 2460 GGACAGAAGC CCAACCTGCT AGACCGACTG CGACACCGCA AAAACGGCTA CCGACACTTG 2520 AAAGACTCCG ACGAAGAAGA GAACGTCTGA 2550 4594 base pairs nucleic acid single linear DNA (genomic) unknown 7 AAGCTTGCGG CCGCTCATTA GACAAGCGAA TGAGGGACGA AAACGTGGAG GAGGTATTAA 60 GTTTGGAGAA ATGGAGAGAG ACTGTTTAAT AGCGCATGGC GCAGCCAATA CTATTACAGA 120 AGTTTTGAAA GATTCGGAAG AAGATTATCA AGATGTGTAT GTTTGTGAAA ATTGTGGAGA 180 CATAGCAGCA CAAATCAAGG GTATTAATAC ATGTCTTAGA TGTTCAAAAC TTAATCTCTC 240 TCCTCTCTTA ACAAAAATTG ATACCACGCA CGTATCTAAA GTATTTCTTA CTCAAATGAA 300 CGCCAGAGGC GTAAAAGTCA AATTAGATTT CGAACGAAGG CCTCCTTCGT TTTATAAACC 360 ATTAGATAAA GTTGATCTCA AGCCGTCTTT TCTGGTGTAA TAAAAATTAA TTAATTACTC 420 GAGGGTACCG GATCCCCCAG CTTATAAAAA TCACAAGACT CTGTCACTTT TTTTGACTAG 480 TTTTTTTTTC TCCTCTTGGT TCAGACGTTC TCTTCTTCGT CGGAGTCTTT CAAGTGTCGG 540 TAGCCGTTTT TGCGGTGTCG CAGTCGGTCT AGCAGGTTGG GCTTCTGTCC CTTGTCCTGC 600 GTGCCAGTCT GTCCGTCCAA AGAATCTGTA CCGTTCTCGT GCGCTCGCTG CTCTGCGTCC 660 AGACGGACCA GGGCCAGAAG CATCTGGTAA GCCTGCTCGT TGGTGTAAGG CGGAGCCGCC 720 GTGGATGCAT CAGACGACGG TGGTCCCGGT CCTTTGCGAC CAGAATTATA AACACTTTCC 780 TCGTAGGAAG GCGGAGCCTG TAACGACGTG TCTTTGGTGT TGCCCGACGT CACGGTGGTC 840 CCGTCGGCGG ACACCAGATA GGGAAAGAGG TTCTGCAGCG GCTGCATGCA GAGACGCCGC 900 TGTCGAGTGT CGTCCAGACC CTTGAGGTAG GGCGGCAGCG GGTCGACTAC CTTGTCCTCC 960 ACGTACTTTA CCCGCTGCTT ATACGAATTG AACTCGCGCA TGATCTCCTC GAGATCAAAA 1020 ACGTTGCTGG AACGCAATTC TTTCTGCGAG TAAAGTTCCA GTACCCTGAA GTCGGTGTTT 1080 TCCAGCGGGT CGATGTCTAG GGCGATCATG CTGTCGACGG TGGAGATGCT GCTGAGGTCA 1140 ATCATGCGTT TGAAGAGGTA GTCCACGTAC TCGTAGGCCG AGTTGCCGGC GATGAAGATC 1200 TTGAGGCTGG GAAGCTGACA TTCCTCAGTG CGGTGGTTGC CCAACAGGAT TTCGTTATCC 1260 TCGCCCAGTT GACCGTACTG CACGTACGAG CTGTTGGCGA AATTAAAGAT GACCACTGGT 1320 CGTGAGTAGC AGCGTCCTGG CGATTCCTTC ACATTCATAT CACGCAGCAC CTTGACGCTG 1380 GTTTGGTTAA TGGTCACGCA GCTGGCCAGA CCCAGGACAT CACCCATGAA ACGCGCGGCA 1440 ATCGGTTTGT TGTAGATGGC CGAGAGAATA GCTGACGGGT TGATCTTGCT AAGTTCCTTG 1500 AAGACCTCTA GGGTGCGCCG TTGATCCACA CACCAGGCTT CTGCGATTTC GGCCAGCGCC 1560 CGGTTGATGT AACCGCGCAA CGTGTCATAG GTGAACTGCA GCTGGGCGTA GACCAGATTG 1620 TGCACCGACT CCATGTTGGA TAAATGAGTT GCATTGTTGC CATCTGTACT TCTTTTGGTT 1680 CTATTATGAG TAAGATTCAG ACTGGAGCGG TTGGCCAAAC GTTCGAGTTC CACCAGAGAT 1740 TTTTGCTTGA TACCTTGCCA GAACACCACC AAACCACCAG TGGTTTCAAA GACGGACACG 1800 TTTCCATATT TTTCATATGT TTGATTGTAT GAAGTATTGA AAATCTGCTG TAACTTATTT 1860 ATGGCCTCAT CACGTACACA GTCCAGCGCA GAGTCGGACA TGTTCACCTC TTGCTTCTTA 1920 GATAAGAAAG TGGCGGTCAT TTTGGCAGAA GAAAAGTGAT ACGAGTCCTC GGCTTCGGAA 1980 CGAATGGTGC GTTCCGAGGC TTCCCAGAAA GTGAGTTGAC AAGTAACATT CTTCTCGTCC 2040 TGTATATCCC AGGAGATCAC TGAGTCCGCA CGTTCAAGAA AAGCCACCAA CCTGTGGGTC 2100 TCTAACGCAG AATTCGGTCT TTCAAAGTCG GAGACGATAG TGTAGTTCGG AAAAATGAAA 2160 AACTTGTCGG CGTTTTCTCC AAAATAGCTG GCATTGCGAT TAGTTCCGTT GTAGAAAGGA 2220 GAAATGTCAA CCACATCACC CGTGGAAGTT GCGAAAAAAT GATAGGGATA CTTGGAGCGC 2280 GCAGTAGTGA TGGTCACCAT ACAATTCAGA TTACAGGTCT CACGATAGAG CCAGGTGCTG 2340 CCGCGGCTGT GCCATTGATC CTTGACCGTC ACGTAACGGG TACTGTGGGT GTTGGAATAA 2400 TCGTCGGGCA TTAATTGCAT GGTTTTGTTT TCATAGCTGT CCCTATGATA AGCCACGAAA 2460 ACCGTGCCTG CTATAACGCG GCTGTAGGAA CTGTAGCACT GACTGTGACT GTTGATATGA 2520 TGAATCTCCC ACATAGGAGG CGCCACGTAT TCCGTGTTGC TGCCCAGCAG ATAAGTGGTG 2580 TGGATGTAAG CGTAGCTACG ACGAAACGTC AAAACCTTCT GGTAGACTCG TACCTTAAAG 2640 GTGTGCGCGA CGATGTTGCG TTTGTAGACC ACCATGATGC CCTCGTCCAG GTCTTCATTG 2700 ATGGGCTTCA TCGAGGTGCA GACGATATTA CGTTCAAAGC GAATAAGATC CGTACCCTGA 2760 GCCATAGAAC ACACGCGATA GGGGTACTTG GTGGTGTTGA CCCCCACCAC ATCTCCGTAC 2820 TTGAGGGTAG TGTTGTAGAT GGTCTCGTTA ACACCATGGC TGACCGTTTG GGAAGAAGTT 2880 ACGCGTTGAG AGACTGAACC GGATCGAGAA TGAGCAGCAG ACGTCGTATG AGAGGAATGG 2940 TGACTGTGAG TAGCAGAAGT TCCACGAGTA GAAGATGAGG AAACCGCAGC ACCCAGACAG 3000 ACGATACACA AGTTAACGCA GACTACCAGG CACCAGATCC TGGATTCCAT TACGATACAA 3060 ACTTAACGGA TATCGCGATA ATGAAATAAT TTATGATTAT TTCTCGCTTT CAATTTAACA 3120 CAACCCTCAA GAACCTTTGT ATTTATTTTC ACTTTTTAAG TATAGAATAA AGAAGCTGGG 3180 AATCGATTCG CGATAGCTGA TTAGTTTTTG TTAACAAAAA TGTGGGAGAA TCTAATTAGT 3240 TTTTCTTTAC ACAATTGACG TACATGAGTC TGAGTTCCTT GTTTTTGCTA ATTATTTCAT 3300 CCAATTTATT ATTCTTGACG ATATCGAGAT CTTTTGTATA GGAGTCAGAC TTGTATTCAA 3360 CATGCTTTTC TATAATCATC TTAGTTATTT CGGCATCATC CAATAGTACA TTTTCCAGAT 3420 TAACAGAGTA GATATTAATG TCGTATTTGA ACAGAGCCTG TAACATCTCA ATGTCTTTAT 3480 TATCTATAGC CAATTTAATG TCCGGAATGA AGAGAAGGGA ATTATTGGTG TTTGTCGACG 3540 TCATATAGTC GAGCAAGAGA ATCATCATAT CCACGTGTCC ATTTTTTATA GTGGTGTGAA 3600 TACAACTAAG GAGAATAGCC AGATCAAAAG TAGATGGTAT TTCTGAAAGA AAGTATGATA 3660 CAATACTTAC ATCATTAAGC ATGACGGCAT GATAAAATGA AGTTTTCCAT CCAGTTTTCC 3720 CATAGAACAT CAGTCTCCAA TTTTTCTTAA ACAGTTTCAC CGTTTGCATG TTACCACTAT 3780 CAACCGCATA ATACAATGCG GTGTTTCCTT TGTCATCAAA TTGTGAATCA TCCATTCCAC 3840 TGAATAGCAA AATCTTTACT ATTTTGGTAT CTTCTAATGT GGCTGCCTGA TGTAATGGAA 3900 ATTCATTCTC TAGAAGATTT TTCAATGCTC CAGCGTTCAA CAACGTACAT ACTAGACGCA 3960 CGTTATTATC AGCTATTGCA TAATACAAGG CACTATGTCC ATGGACATCC GCCTTAAATG 4020 TATCTTTACT AGAGAGAAAG CTTTTCAGCT GCTTAGACTT CCAAGTATTA ATTCGTGACA 4080 GATCCATGTC TGAAACGAGA CGCTAATTAG TGTATATTTT TTCATTTTTT ATAATTTTGT 4140 CATATTGCAC CAGAATTAAT AATATCTCTA ATAGATCTAA TTTAATTTAA TTTATATAAC 4200 TTATTTTTTG AATATACTTT TAATTAACAA AAGAGTTAAG TTACTCATAT GGACGCCGTC 4260 CAGTCTGAAC ATCAATCTTT TTAGCCAGAG ATATCATAGC CGCTCTTAGA GTTTCAGCGT 4320 GATTTTCCAA CCTAAATAGA ACTTCATCGT TGCGTTTACA ACACTTTTCT ATTTGTTCAA 4380 ACTTTGTTGT TACATTAGTA ATCTTTTTTT CCAAATTAGT TAGCCGTTGT TTGAGAGTTT 4440 CCTCATTGTC GTCTTCATCG GCTTTAACAA TTGCTTCGCG TTTAGCCTCC TGGCTGTTCT 4500 TATCAGCCTT TGTAGAAAAA AATTCAGTTG CTGGAATTGC AAGATCGTCA TCTCCGGGGA 4560 AAAGAGTTCC GTCCATTTAA AGCCGCGGGA ATTC 4594 2550 base pairs nucleic acid single linear DNA (genomic) unknown 8 ATGGAATCCA GGATCTGGTG CCTGGTAGTC TGCGTTAACT TGTGTATCGT CTGTCTGGGT 60 GCTGCGGTTT CCTCATCTTC TACTCGTGGA ACTTCTGCTA CTCACAGTCA CCATTCCTCT 120 CATACGACGT CTGCTGCTCA TTCTCGATCC GGTTCAGTCT CTCAACGCGT AACTTCTTCC 180 CAAACGGTCA GCCATGGTGT TAACGAGACC ATCTACAACA CTACCCTCAA GTACGGAGAT 240 GTGGTGGGGG TCAACACCAC CAAGTACCCC TATCGCGTGT GTTCTATGGC TCAGGGTACG 300 GATCTTATTC GCTTTGAACG TAATATCGTC TGCACCTCGA TGAAGCCCAT CAATGAAGAC 360 CTGGACGAGG GCATCATGGT GGTCTACAAA CGCAACATCG TCGCGCACAC CTTTAAGGTA 420 CGAGTCTACC AGAAGGTTTT GACGTTTCGT CGTAGCTACG CTTACATCCA CACCACTTAT 480 CTGCTGGGCA GCAACACGGA ATACGTGGCG CCTCCTATGT GGGAGATTCA TCATATCAAC 540 AGTCACAGTC AGTGCTACAG TTCCTACAGC CGCGTTATAG CAGGCACGGT TTTCGTGGCT 600 TATCATAGGG ACAGCTATGA AAACAAAACC ATGCAATTAA TGCCCGACGA TTATTCCAAC 660 ACCCACAGTA CCCGTTACGT GACGGTCAAG GATCAATGGC ACAGCCGCGG CAGCACCTGG 720 CTCTATCGTG AGACCTGTAA TCTGAATTGT ATGGTGACCA TCACTACTGC GCGCTCCAAG 780 TATCCCTATC ATTTTTTCGC AACTTCCACG GGTGATGTGG TTGACATTTC TCCTTTCTAC 840 AACGGAACTA ATCGCAATGC CAGCTATTTT GGAGAAAACG CCGACAAGTT TTTCATTTTT 900 CCGAACTACA CTATCGTCTC CGACTTTGAA AGACCGAATT CTGCGTTAGA GACCCACAGG 960 TTGGTGGCTT TTCTTGAACG TGCGGACTCA GTGATCTCCT GGGATATACA GGACGAGAAG 1020 AATGTTACTT GTCAACTCAC TTTCTGGGAA GCCTCGGAAC GCACCATTCG TTCCGAAGCC 1080 GAGGACTCGT ATCACTTTTC TTCTGCCAAA ATGACCGCCA CTTTCTTATC TAAGAAGCAA 1140 GAGGTGAACA TGTCCGACTC TGCGCTGGAC TGTGTACGTG ATGAGGCCAT AAATAAGTTA 1200 CAGCAGATTT TCAATACTTC ATACAATCAA ACATATGAAA AATATGGAAA CGTGTCCGTC 1260 TTTGAAACCA CTGGTGGTTT GGTGGTGTTC TGGCAAGGTA TCAAGCAAAA ATCTCTGGTG 1320 GAACTCGAAC GTTTGGCCAA CCGCTCCAGT CTGAATCTTA CTCATAATAG AACCATAAGA 1380 TCTACAGATG GCAACAATGC AACTCATTTA TCCAACATGG AGTCGGTGCA CAATCTGGTC 1440 TACGCCCAGC TGCAGTTCAC CTATGACACG TTGCGCGGTT ACATCAACCG GGCGCTGGCC 1500 GAAATCGCAG AAGCCTGGTG TGTGGATCAA CGGCGCACCC TAGAGGTCTT CAAGGAACTT 1560 AGCAAGATCA ACCCGTCAGC TATTCTCTCG GCCATCTACA ACAAACCGAT TGCCGCGCGT 1620 TTCATGGGTG ATGTCCTGGG TCTGGCCAGC TGCGTGACCA TTAACCAAAC CAGCGTCAAG 1680 GTGCTGCGTG ATATGAATGT GAAGGAATCG CCAGGACGCT GCTACTCACG ACCAGTGGTC 1740 ATCTTTAATT TCGCCAACAG CTCGTACGTG CAGTACGGTC AACTGGGCGA GGATAACGAA 1800 ATCCTGTTGG GCAACCACCG CACTGAGGAA TGTCAGCTTC CCAGCCTCAA GATCTTCATC 1860 GCCGGCAACT CGGCCTACGA GTACGTGGAC TACCTCTTCA AACGCATGAT TGACCTCAGC 1920 AGCATCTCCA CCGTCGACAG CATGATCGCC CTAGACATCG ACCCGCTGGA AAACACCGAC 1980 TTCAGGGTAC TGGAACTTTA CTCGCAGAAA GAATTGCGTT CCAGCAACGT TTTTGATCTC 2040 GAGGAGATCA TGCGCGAGTT CAATTCGTAT AAGCAGCGGG TAAAGTACGT GGAGGACAAG 2100 GTAGTCGACC CGCTGCCGCC CTACCTCAAG GGTCTGGACG ACACTCGACA GCGGCGTCTC 2160 TGCATGCAGC CGCTGCAGAA CCTCTTTCCC TATCTGGTGT CCGCCGACGG GACCACCGTG 2220 ACGTCGGGCA ACACCAAAGA CACGTCGTTA CAGGCTCCGC CTTCCTACGA GGAAAGTGTT 2280 TATAATTCTG GTCGCAAAGG ACCGGGACCA CCGTCGTCTG ATGCATCCAC GGCGGCTCCG 2340 CCTTACACCA ACGAGCAGGC TTACCAGATG CTTCTGGCCC TGGTCCGTCT GGACGCAGAG 2400 CAGCGAGCGC ACGAGAACGG TACAGATTCT TTGGACGGAC AGACTGGCAC GCAGGACAAG 2460 GGACAGAAGC CCAACCTGCT AGACCGACTG CGACACCGCA AAAACGGCTA CCGACACTTG 2520 AAAGACTCCG ACGAAGAAGA GAACGTCTGA 2550 4594 base pairs nucleic acid single linear DNA (genomic) unknown 9 AAGCTTGCGG CCGCTCATTA GACAAGCGAA TGAGGGACGA AAACGTGGAG GAGGTATTAA 60 GTTTGGAGAA ATGGAGAGAG ACTGTTTAAT AGCGCATGGC GCAGCCAATA CTATTACAGA 120 AGTTTTGAAA GATTCGGAAG AAGATTATCA AGATGTGTAT GTTTGTGAAA ATTGTGGAGA 180 CATAGCAGCA CAAATCAAGG GTATTAATAC ATGTCTTAGA TGTTCAAAAC TTAATCTCTC 240 TCCTCTCTTA ACAAAAATTG ATACCACGCA CGTATCTAAA GTATTTCTTA CTCAAATGAA 300 CGCCAGAGGC GTAAAAGTCA AATTAGATTT CGAACGAAGG CCTCCTTCGT TTTATAAACC 360 ATTAGATAAA GTTGATCTCA AGCCGTCTTT TCTGGTGTAA TAAAAATTAA TTAATTACTC 420 GAGGGTACCG GATCCCCCAG CTTATAAAAA TCACAAGTCT CTGACACTTT TTTTGTCTAG 480 TTTTTTTTTC TCCTCTTGGT TCAGACGTTC TCTTCTTCGT CGGAGTCTTT CAAGTGTCGG 540 TAGCCGTTTT TGCGGTGTCG CAGTCGGTCT AGCAGGTTGG GCTTCTGTCC CTTGTCCTGC 600 GTGCCAGTCT GTCCGTCCAA AGAATCTGTA CCGTTCTCGT GCGCTCGCTG CTCTGCGTCC 660 AGACGGACCA GGGCCAGAAG CATCTGGTAA GCCTGCTCGT TGGTGTAAGG CGGAGCCGCC 720 GTGGATGCAT CAGACGACGG TGGTCCCGGT CCTTTGCGAC CAGAATTATA AACACTTTCC 780 TCGTAGGAAG GCGGAGCCTG TAACGACGTG TCTTTGGTGT TGCCCGACGT CACGGTGGTC 840 CCGTCGGCGG ACACCAGATA GGGAAAGAGG TTCTGCAGCG GCTGCATGCA GAGACGCCGC 900 TGTCGAGTGT CGTCCAGACC CTTGAGGTAG GGCGGCAGCG GGTCGACTAC CTTGTCCTCC 960 ACGTACTTTA CCCGCTGCTT ATACGAATTG AACTCGCGCA TGATCTCCTC GAGATCAAAA 1020 ACGTTGCTGG AACGCAATTC TTTCTGCGAG TAAAGTTCCA GTACCCTGAA GTCGGTGTTT 1080 TCCAGCGGGT CGATGTCTAG GGCGATCATG CTGTCGACGG TGGAGATGCT GCTGAGGTCA 1140 ATCATGCGTT TGAAGAGGTA GTCCACGTAC TCGTAGGCCG AGTTGCCGGC GATGAAGATC 1200 TTGAGGCTGG GAAGCTGACA TTCCTCAGTG CGGTGGTTGC CCAACAGGAT TTCGTTATCC 1260 TCGCCCAGTT GACCGTACTG CACGTACGAG CTGTTGGCGA AATTAAAGAT GACCACTGGT 1320 CGTGAGTAGC AGCGTCCTGG CGATTCCTTC ACATTCATAT CACGCAGCAC CTTGACGCTG 1380 GTTTGGTTAA TGGTCACGCA GCTGGCCAGA CCCAGGACAT CACCCATGAA ACGCGCGGCA 1440 ATCGGTTTGT TGTAGATGGC CGAGAGAATA GCTGACGGGT TGATCTTGCT AAGTTCCTTG 1500 AAGACCTCTA GGGTGCGCCG TTGATCCACA CACCAGGCTT CTGCGATTTC GGCCAGCGCC 1560 CGGTTGATGT AACCGCGCAA CGTGTCATAG GTGAACTGCA GCTGGGCGTA GACCAGATTG 1620 TGCACCGACT CCATGTTGGA TAAATGAGTT GCATTGTTGC CATCTGTAGA TCTTATGGTT 1680 CTATTATGAG TAAGATTCAG ACTGGAGCGG TTGGCCAAAC GTTCGAGTTC CACCAGAGAT 1740 TTTTGCTTGA TACCTTGCCA GAACACCACC AAACCACCAG TGGTTTCAAA GACGGACACG 1800 TTTCCATATT TTTCATATGT TTGATTGTAT GAAGTATTGA AAATCTGCTG TAACTTATTT 1860 ATGGCCTCAT CACGTACACA GTCCAGCGCA GAGTCGGACA TGTTCACCTC TTGCTTCTTA 1920 GATAAGAAAG TGGCGGTCAT TTTGGCAGAA GAAAAGTGAT ACGAGTCCTC GGCTTCGGAA 1980 CGAATGGTGC GTTCCGAGGC TTCCCAGAAA GTGAGTTGAC AAGTAACATT CTTCTCGTCC 2040 TGTATATCCC AGGAGATCAC TGAGTCCGCA CGTTCAAGAA AAGCCACCAA CCTGTGGGTC 2100 TCTAACGCAG AATTCGGTCT TTCAAAGTCG GAGACGATAG TGTAGTTCGG AAAAATGAAA 2160 AACTTGTCGG CGTTTTCTCC AAAATAGCTG GCATTGCGAT TAGTTCCGTT GTAGAAAGGA 2220 GAAATGTCAA CCACATCACC CGTGGAAGTT GCGAAAAAAT GATAGGGATA CTTGGAGCGC 2280 GCAGTAGTGA TGGTCACCAT ACAATTCAGA TTACAGGTCT CACGATAGAG CCAGGTGCTG 2340 CCGCGGCTGT GCCATTGATC CTTGACCGTC ACGTAACGGG TACTGTGGGT GTTGGAATAA 2400 TCGTCGGGCA TTAATTGCAT GGTTTTGTTT TCATAGCTGT CCCTATGATA AGCCACGAAA 2460 ACCGTGCCTG CTATAACGCG GCTGTAGGAA CTGTAGCACT GACTGTGACT GTTGATATGA 2520 TGAATCTCCC ACATAGGAGG CGCCACGTAT TCCGTGTTGC TGCCCAGCAG ATAAGTGGTG 2580 TGGATGTAAG CGTAGCTACG ACGAAACGTC AAAACCTTCT GGTAGACTCG TACCTTAAAG 2640 GTGTGCGCGA CGATGTTGCG TTTGTAGACC ACCATGATGC CCTCGTCCAG GTCTTCATTG 2700 ATGGGCTTCA TCGAGGTGCA GACGATATTA CGTTCAAAGC GAATAAGATC CGTACCCTGA 2760 GCCATAGAAC ACACGCGATA GGGGTACTTG GTGGTGTTGA CCCCCACCAC ATCTCCGTAC 2820 TTGAGGGTAG TGTTGTAGAT GGTCTCGTTA ACACCATGGC TGACCGTTTG GGAAGAAGTT 2880 ACGCGTTGAG AGACTGAACC GGATCGAGAA TGAGCAGCAG ACGTCGTATG AGAGGAATGG 2940 TGACTGTGAG TAGCAGAAGT TCCACGAGTA GAAGATGAGG AAACCGCAGC ACCCAGACAG 3000 ACGATACACA AGTTAACGCA GACTACCAGG CACCAGATCC TGGATTCCAT TACGATACAA 3060 ACTTAACGGA TATCGCGATA ATGAAATAAT TTATGATTAT TTCTCGCTTT CAATTTAACA 3120 CAACCCTCAA GAACCTTTGT ATTTATTTTC ACTTTTTAAG TATAGAATAA AGAAGCTGGG 3180 AATCGATTCG CGATAGCTGA TTAGTTTTTG TTAACAAAAA TGTGGGAGAA TCTAATTAGT 3240 TTTTCTTTAC ACAATTGACG TACATGAGTC TGAGTTCCTT GTTTTTGCTA ATTATTTCAT 3300 CCAATTTATT ATTCTTGACG ATATCGAGAT CTTTTGTATA GGAGTCAGAC TTGTATTCAA 3360 CATGCTTTTC TATAATCATC TTAGTTATTT CGGCATCATC CAATAGTACA TTTTCCAGAT 3420 TAACAGAGTA GATATTAATG TCGTATTTGA ACAGAGCCTG TAACATCTCA ATGTCTTTAT 3480 TATCTATAGC CAATTTAATG TCCGGAATGA AGAGAAGGGA ATTATTGGTG TTTGTCGACG 3540 TCATATAGTC GAGCAAGAGA ATCATCATAT CCACGTGTCC ATTTTTTATA GTGGTGTGAA 3600 TACAACTAAG GAGAATAGCC AGATCAAAAG TAGATGGTAT TTCTGAAAGA AAGTATGATA 3660 CAATACTTAC ATCATTAAGC ATGACGGCAT GATAAAATGA AGTTTTCCAT CCAGTTTTCC 3720 CATAGAACAT CAGTCTCCAA TTTTTCTTAA ACAGTTTCAC CGTTTGCATG TTACCACTAT 3780 CAACCGCATA ATACAATGCG GTGTTTCCTT TGTCATCAAA TTGTGAATCA TCCATTCCAC 3840 TGAATAGCAA AATCTTTACT ATTTTGGTAT CTTCTAATGT GGCTGCCTGA TGTAATGGAA 3900 ATTCATTCTC TAGAAGATTT TTCAATGCTC CAGCGTTCAA CAACGTACAT ACTAGACGCA 3960 CGTTATTATC AGCTATTGCA TAATACAAGG CACTATGTCC ATGGACATCC GCCTTAAATG 4020 TATCTTTACT AGAGAGAAAG CTTTTCAGCT GCTTAGACTT CCAAGTATTA ATTCGTGACA 4080 GATCCATGTC TGAAACGAGA CGCTAATTAG TGTATATTTT TTCATTTTTT ATAATTTTGT 4140 CATATTGCAC CAGAATTAAT AATATCTCTA ATAGATCTAA TTTAATTTAA TTTATATAAC 4200 TTATTTTTTG AATATACTTT TAATTAACAA AAGAGTTAAG TTACTCATAT GGACGCCGTC 4260 CAGTCTGAAC ATCAATCTTT TTAGCCAGAG ATATCATAGC CGCTCTTAGA GTTTCAGCGT 4320 GATTTTCCAA CCTAAATAGA ACTTCATCGT TGCGTTTACA ACACTTTTCT ATTTGTTCAA 4380 ACTTTGTTGT TACATTAGTA ATCTTTTTTT CCAAATTAGT TAGCCGTTGT TTGAGAGTTT 4440 CCTCATTGTC GTCTTCATCG GCTTTAACAA TTGCTTCGCG TTTAGCCTCC TGGCTGTTCT 4500 TATCAGCCTT TGTAGAAAAA AATTCAGTTG CTGGAATTGC AAGATCGTCA TCTCCGGGGA 4560 AAAGAGTTCC GTCCATTTAA AGCCGCGGGA ATTC 4594 2229 base pairs nucleic acid single linear DNA (genomic) unknown 10 ATGCGGCCAG GCCTCCCCTC CTACCTCATC GTCCTCGCCG TCTGTCTCCT CAGCCACCTA 60 CTTTCGTCAC GATATGGCGC AGAAGCCATA TCCGAACCGC TGGACAAAGC GTTTCACCTA 120 CTGCTCAACA CCTACGGGAG ACCCATCCGC TTCCTGCGTG AAAACACCAC CCAGTGTACC 180 TACAATAGCA GCCTCCGTAA CAGCACGGTC GTCAGGGAAA ACGCCATCAG TTTCAACTTT 240 TTCCAAAGCT ATAATCAATA CTATGTATTC CATATGCCTC GATGTCTTTT TGCGGGTCCT 300 CTGGCGGAGC AGTTTCTGAA CCAGGTAGAT CTGACCGAAA CCCTGGAAAG ATACCAACAG 360 AGACTTAACA CTTACGCGCT GGTATCCAAA GACCTGGCCA GCTACCGATC TTTTTCGCAG 420 CAGCTAAAGG CACAGGACAG CCTAGGTGAA CAGCCCACCA CTGTGCCACC ACCCATTGAC 480 CTGTCAATAC CTCACGTTTG GATGCCACCG CAAACCACTC CACACGGCTG GACAGAATCA 540 CATACCACCT CAGGACTACA CCGACCACAC TTTAACCAGA CCTGTATCCT CTTTGATGGA 600 CACGATCTAC TATTCAGCAC CGTCACACCT TGTTTGCACC AAGGCTTTTA CCTCATCGAC 660 GAACTACGTT ACGTTAAAAT AACACTGACC GAGGACTTCT TCGTAGTTAC GGTGTCCATA 720 GACGACGACA CACCCATGCT GCTTATCTTC GGCCATCTTC CACGCGTACT CTTTAAAGCG 780 CCCTATCAAC GCGACAACTT TATACTACGA CAAACTGAAA AACACGAGCT CCTGGTGCTA 840 GTTAAGAAAG ATCAACTGAA CCGTCACTCT TATCTCAAAG ACCCGGACTT TCTTGACGCC 900 GCACTTGACT TCAACTACCT GGACCTCAGC GCACTACTAC GTAACAGCTT TCACCGTTAC 960 GCCGTGGATG TACTCAAAAG CGGTCGATGT CAGATGCTGG ACCGCCGCAC GGTAGAAATG 1020 GCCTTCGCCT ACGCATTAGC ACTGTTCGCA GCAGCCCGAC AAGAAGAGGC CGGCGCCCAA 1080 GTCTCCGTCC CACGGGCCCT AGACCGCCAG GCCGCACTCT TACAAATACA AGAATTTATG 1140 ATCACCTGCC TCTCACAAAC ACCACCACGC ACCACGTTGC TGCTGTATCC CACGGCCGTG 1200 GACCTGGCCA AACGAGCCCT TTGGACACCG AATCAGATCA CCGACATCAC CAGCCTCGTA 1260 CGCCTGGTCT ACATACTCTC TAAACAGAAT CAGCAACATC TCATCCCCCA GTGGGCACTA 1320 CGACAGATCG CCGACTTTGC CCTAAAACTA CACAAAACGC ACCTGGCCTC TTTTCTTTCA 1380 GCCTTCGCGC GTCAAGAACT CTACCTCATG GGCAGCCTCG TCCACTCCAT GCTAGTACAT 1440 ACGACGGAGA GACGCGAAAT CTTCATCGTA GAAACGGGCC TCTGTTCATT AGCCGAGCTA 1500 TCACACTTTA CGCAGTTGCT AGCTCATCCG CACCACGAAT ACCTCAGCGA CCTGTACACA 1560 CCCTGTTCCA GTAGCGGGCG ACGCGATCAC TCGCTCGAAC GCCTCACACG TCTCTTCCCC 1620 GATGCCACCG TCCCCACTAC CGTTCCCGCC GCCCTCTCCA TCCTATCTAC CATGCAACCA 1680 AGCACGCTAG AAACCTTCCC CGACCTGTTT TGTCTGCCGC TCGGCGAATC CTTCTCCGCG 1740 CTGACCGTCT CCGAACACGT CAGTTATGTC GTAACAAACC AGTACCTGAT CAAAGGTATC 1800 TCCTACCCTG TCTCCACCAC CGTCGTAGGC CAGAGCCTCA TCATCACCCA GACGGACAGT 1860 CAAACTAAAT GCGAACTGAC GCGCAACATG CATACCACAC ACAGCATCAC AGCGGCGCTC 1920 AACATTTCCC TAGAAAACTG CGCCTTTTGC CAAAGCGCCC TACTAGAATA CGACGACACG 1980 CAAGGCGTCA TCAACATCAT GTACATGCAC GACTCGGACG ACGTCCTTTT CGCCCTGGAT 2040 CCCTACAACG AAGTGGTGGT CTCATCTCCG CGAACTCACT ACCTCATGCT TTTGAAAAAC 2100 GGTACGGTCC TAGAAGTAAC TGACGTCGTC GTGGACGCTA CCGACAGTCG TCTCCTCATG 2160 ATGTCCGTCT ACGCGCTATC GGCCATCATC GGCATCTATC TGCTCTACCG CATGCTCAAG 2220 ACATGCTGA 2229 3539 base pairs nucleic acid single linear DNA (genomic) unknown 11 CTGCAGGTCG ACGGATCTGA GAATGGATGA TTCTCCAGCC GAAACATATT CTACCATGGC 60 TCCGTTTAAT TTGTTGATGA AGATGGATTC ATCCTTAAAT GTTTTCTCTG TAATAGTTTC 120 CACCGAAAGA CTATGCAAAG AATTTGGAAT GCGTTCCTTG TGCTTAATGT TTCCATAGAC 180 GGCTTCTAGA AGTTGATACA ACATAGGACT AGCCGCGGTA ACTTTTATTT TTAGAAAGTA 240 TCCATCGCTT CTATCTTGTT TAGATTTATT TTTATAAAGT TTAGTCTCTC CTTCCAACAT 300 AATAAAAGTG GAAGTCATTT GACTAGATAA ACTATCAGTA AGTTTTATAG AGATAGACGA 360 ACAATTAGCG TATTGAGAAG CATTTAGTGT AACGTATTCG ATACATTTTG CATTAGATTT 420 ACTAATCGAT TTTGCATACT CTATAACACC CGCACAAGTC TGTAGAGAAT CGCTAGATGC 480 AGTAGGTCTT GGTGAAGTTT CAACTCTCTT CTTGATTACC TTACTCATGA TTAAACCTAA 540 ATAATTGTAC TTTGTAATAT AATGATATAT ATTTTCACTT TATCTCATTT GAGAATAAAA 600 AGATCACAAA AATTAACTAA TCAGGATCCG GTACCCTCGA GTTTATTGGG AAGAATATGA 660 TAATATTTTG GGATTTCAAA ATTGAAAATA TATAATTACA ATATAAAATG CGGCCCGGGC 720 TCCCCTCCTA CCTCATCGTC CTCGCCGTCT GTCTCCTCAG CCACCTACTT TCGTCACGAT 780 ATGGCGCAGA AGCCATATCC GAACCGCTGG ACAAAGCGTT TCACCTACTG CTCAACACCT 840 ACGGGAGACC CATCCGCTTC CTGCGTGAAA ACACCACCCA GTGTACCTAC AATAGCAGCC 900 TCCGTAACAG CACGGTCGTC AGGGAAAACG CCATCAGTTT CAACTTTTTC CAAAGCTATA 960 ATCAATACTA TGTATTCCAT ATGCCTCGAT GTCTTTTTGC GGGTCCTCTG GCGGAGCAGT 1020 TTCTGAACCA GGTAGATCTG ACCGAAACCC TGGAAAGATA CCAACAGAGA CTTAACACTT 1080 ACGCGCTGGT ATCCAAAGAC CTGGCCAGCT ACCGATCTTT TTCGCAGCAG CTAAAGGCAC 1140 AGGACAGCCT AGGTGAACAG CCCACCACTG TGCCACCACC CATTGACCTG TCAATACCTC 1200 ACGTTTGGAT GCCACCGCAA ACCACTCCAC ACGGCTGGAC AGAATCACAT ACCACCTCAG 1260 GACTACACCG ACCACACTTT AACCAGACCT GTATCCTCTT TGATGGACAC GATCTACTAT 1320 TCAGCACCGT CACACCTTGT TTGCACCAAG GCTTTTACCT CATCGACGAA CTACGTTACG 1380 TTAAAATAAC ACTGACCGAG GACTTCTTCG TAGTTACGGT GTCCATAGAC GACGACACAC 1440 CCATGCTGCT TATCTTCGGC CATCTTCCAC GCGTACTCTT TAAAGCGCCC TATCAACGCG 1500 ACAACTTTAT ACTACGACAA ACTGAAAAAC ACGAGCTCCT GGTGCTAGTT AAGAAAGATC 1560 AACTGAACCG TCACTCTTAT CTCAAAGACC CGGACTTTCT TGACGCCGCA CTTGACTTCA 1620 ACTACCTGGA CCTCAGCGCA CTACTACGTA ACAGCTTTCA CCGTTACGCC GTGGATGTAC 1680 TCAAAAGCGG TCGATGTCAG ATGCTGGACC GCCGCACGGT AGAAATGGCC TTCGCCTACG 1740 CATTAGCACT GTTCGCAGCA GCCCGACAAG AAGAGGCCGG CGCCCAAGTC TCCGTCCCAC 1800 GGGCCCTAGA CCGCCAGGCC GCACTCTTAC AAATACAAGA ATTTATGATC ACCTGCCTCT 1860 CACAAACACC ACCACGCACC ACGTTGCTGC TGTATCCCAC GGCCGTGGAC CTGGCCAAAC 1920 GAGCCCTTTG GACACCGAAT CAGATCACCG ACATCACCAG CCTCGTACGC CTGGTCTACA 1980 TACTCTCTAA ACAGAATCAG CAACATCTCA TCCCCCAGTG GGCACTACGA CAGATCGCCG 2040 ACTTTGCCCT AAAACTACAC AAAACGCACC TGGCCTCTTT TCTTTCAGCC TTCGCGCGTC 2100 AAGAACTCTA CCTCATGGGC AGCCTCGTCC ACTCCATGCT AGTACATACG ACGGAGAGAC 2160 GCGAAATCTT CATCGTAGAA ACGGGCCTCT GTTCATTAGC CGAGCTATCA CACTTTACGC 2220 AGTTGCTAGC TCATCCGCAC CACGAATACC TCAGCGACCT GTACACACCC TGTTCCAGTA 2280 GCGGGCGACG CGATCACTCG CTCGAACGCC TCACACGTCT CTTCCCCGAT GCCACCGTCC 2340 CCACTACCGT TCCCGCCGCC CTCTCCATCC TATCTACCAT GCAACCAAGC ACGCTAGAAA 2400 CCTTCCCCGA CCTGTTTTGT CTGCCGCTCG GCGAATCCTT CTCCGCGCTG ACCGTCTCCG 2460 AACACGTCAG TTATGTCGTA ACAAACCAGT ACCTGATCAA AGGTATCTCC TACCCTGTCT 2520 CCACCACCGT CGTAGGCCAG AGCCTCATCA TCACCCAGAC GGACAGTCAA ACTAAATGCG 2580 AACTGACGCG CAACATGCAT ACCACACACA GCATCACAGC GGCGCTCAAC ATTTCCCTAG 2640 AAAACTGCGC CTTTTGCCAA AGCGCCCTAC TAGAATACGA CGACACGCAA GGCGTCATCA 2700 ACATCATGTA CATGCACGAC TCGGACGACG TCCTTTTCGC CCTGGATCCC TACAACGAAG 2760 TGGTGGTCTC ATCTCCGCGA ACTCACTACC TCATGCTTTT GAAAAACGGT ACGGTCCTAG 2820 AAGTAACTGA CGTCGTCGTG GACGCTACCG ACAGTCGTCT CCTCATGATG TCCGTCTACG 2880 CGCTATCGGC CATCATCGGC ATCTATCTGC TCTACCGCAT GCTCAAGACA TGCTGATTTT 2940 TATCTCGAGC CCGGGAGATC TTAGCTAACT GATTTTTCTG GGAAAAAAAT TATTTAACTT 3000 TTCATTAATA GGGATTTGAC GTATGTAGCG TACAAAATTA TCGTTCCTGG TATATAGATA 3060 AAGAGTCCTA TATATTTGAA AATCGTTACG GCTCGATTAA ACTTTAATGA TTGCATAGTG 3120 AATATATCAT TAGGATTTAA CTCCTTGACT ATCATGGCGG CGCCAGAAAT TACCATCAAA 3180 AGCATTAATA CAGTTATGCC GATCGCAGTT AGAACGGTTA TAGCATCCAC CATTTATATC 3240 TAAAAATTAG ATCAAAGAAT ATGTGACAAA GTCCTAGTTG TATACTGAGA ATTGACGAAA 3300 CAATGTTTCT TACATATTTT TTTCTTATTA GTAACTGACT TAATAGTAGG AACTGGAAAG 3360 CTAGACTTGA TTATTCTATA AGTATAGATA CCCTTCCAGA TAATGTTCTC TTTGATAAAA 3420 GTTCCAGAAA ATGTAGAATT TTTTAAAAAG TTATCTTTTG CTATTACCAA GATTGTGTTT 3480 AGACGCTTAT TATTAATATG AGTAATGAAA TCCACACCGC CTCTAGATAT GGGGAATTC 3539 4427 base pairs nucleic acid single linear DNA (genomic) unknown 12 GAATTGCGGC CGCTGAATGT TAAATGTTAT ACTTTGGATG AAGCTATAAA TATGCATTGG 60 AAAAATAATC CATTTAAAGA AAGGATTCAA ATACTACAAA ACCTAAGCGA TAATATGTTA 120 ACTAAGCTTA TTCTTAACGA CGCTTTAAAT ATACACAAAT AAACATAATT TTTGTATAAC 180 CTAACAAATA ACTAAAACAT AAAAATAATA AAAGGAAATG TAATATCGTA ATTATTTTAC 240 TCAGGAATGG GGTTAAATAT TTATATCACG TGTATATCTA TACTGTTATC GTATACTCTT 300 TACAATTACT ATTACGAATA TGCAAGAGAT AATAAGATTA CGTATTTAAG AGAATCTTCT 360 CATGATAATT GGGTACGACA TAGTGATAAA TGCTATTTCG CATCGTTACA TAAAGTCAGT 420 TGGAAAGATG GATTTGACAG ATGTAACTTA ATAGGTGCAA AAATGTTAAA TAACAGCATT 480 CTATCGGAAG ATAGGATACC AGTTATATTA TACAAAAATC ACTGGTTGGA TAAAACAGAT 540 TCTGCAATAT TCGTAAAAGA TGAAGATTAC TGCGAATTTG TAAACTATGA CAATAAAAAG 600 CCATTTATCT CAACGACATC GTGTAATTCT TCCATGTTTT ATGTATGTGT TTCAGATATT 660 ATGAGATTAC TATAAACTTT TTGTATACTT ATATTCCGTA AACTATATTA ATCATGAAGA 720 AAATGAAAAA GTATAGAAGC TGTTCACGAG CGGTTGTTGA AAACAACAAA ATTATACATT 780 CAAGATGGCT TACATATACG TCTGTGAGGC TATCATGGAT AATGACAATG CATCTCTAAA 840 TAGGTTTTTG GACAATGGAT TCGACCCTAA CACGGAATAT GGTACTCTAC AATCTCCTCT 900 TGAAATGGCT GTAATGTTCA AGAATACCGA GGCTATAAAA ATCTTGATGA GGTATGGAGC 960 TAAACCTGTA GTTACTGAAT GCACAACTTC TTGTCTGCAT GATGCGGTGT TGAGAGACGA 1020 CTACAAAATA GTGAAAGATC TGTTGAAGAA TAACTATGTA AACAATGTTC TTTACAGCGG 1080 AGGCTTTACT CCTTTGTGTT TGGCAGCTTA CCTTAACAAA GTTAATTTGG TTAAACTTCT 1140 ATTGGCTCAT TCGGCGGATG TAGATATTTC AAACACGGAT CGGTTAACTC CTCTACATAT 1200 AGCCGTATCA AATAAAAATT TAACAATGGT TAAACTTCTA TTGAACAAAG GTGCTGATAC 1260 TGACTTGCTG GATAACATGG GACGTACTCC TTTAATGATC GCTGTACAAT CTGGAAATAT 1320 TGAAATATGT AGCACACTAC TTAAAAAAAA TAAAATGTCC AGAACTGGGA AAAATTGATC 1380 TTGCCAGCTG TAATTCATGG TAGAAAAGAA GTGCTCAGGC TACTTTTCAA CAAAGGAGCA 1440 GATGTAAACT ACATCTTTGA AAGAAATGGA AAATCATATA CTGTTTTGGA ATTGATTAAA 1500 GAAAGTTACT CTGAGACACA AAAGAGGTAG CTGAAGTGGT ACTCTCAAAG GTACGTGACT 1560 AATTAGCTAT AAAAAGGATC TTAATTAATT AGTCATCAGG CAGGGCGAGA ACGAGACTAT 1620 CTGCTCGTTA ATTAATTAGG TCGACGGATC CGGTACCCTC GAGTTTATTG GGAAGAATAT 1680 GATAATATTT TGGGATTTCA AAATTGAAAA TATATAATTA CAATATAAAA TGCGGCCCGG 1740 GCTCCCCTCC TACCTCATCG TCCTCGCCGT CTGTCTCCTC AGCCACCTAC TTTCGTCACG 1800 ATATGGCGCA GAAGCCATAT CCGAACCGCT GGACAAAGCG TTTCACCTAC TGCTCAACAC 1860 CTACGGGAGA CCCATCCGCT TCCTGCGTGA AAACACCACC CAGTGTACCT ACAATAGCAG 1920 CCTCCGTAAC AGCACGGTCG TCAGGGAAAA CGCCATCAGT TTCAACTTTT TCCAAAGCTA 1980 TAATCAATAC TATGTATTCC ATATGCCTCG ATGTCTTTTT GCGGGTCCTC TGGCGGAGCA 2040 GTTTCTGAAC CAGGTAGATC TGACCGAAAC CCTGGAAAGA TACCAACAGA GACTTAACAC 2100 TTACGCGCTG GTATCCAAAG ACCTGGCCAG CTACCGATCT TTTTCGCAGC AGCTAAAGGC 2160 ACAGGACAGC CTAGGTGAAC AGCCCACCAC TGTGCCACCA CCCATTGACC TGTCAATACC 2220 TCACGTTTGG ATGCCACCGC AAACCACTCC ACACGGCTGG ACAGAATCAC ATACCACCTC 2280 AGGACTACAC CGACCACACT TTAACCAGAC CTGTATCCTC TTTGATGGAC ACGATCTACT 2340 ATTCAGCACC GTCACACCTT GTTTGCACCA AGGCTTTTAC CTCATCGACG AACTACGTTA 2400 CGTTAAAATA ACACTGACCG AGGACTTCTT CGTAGTTACG GTGTCCATAG ACGACGACAC 2460 ACCCATGCTG CTTATCTTCG GCCATCTTCC ACGCGTACTC TTTAAAGCGC CCTATCAACG 2520 CGACAACTTT ATACTACGAC AAACTGAAAA ACACGAGCTC CTGGTGCTAG TTAAGAAAGA 2580 TCAACTGAAC CGTCACTCTT ATCTCAAAGA CCCGGACTTT CTTGACGCCG CACTTGACTT 2640 CAACTACCTG GACCTCAGCG CACTACTACG TAACAGCTTT CACCGTTACG CCGTGGATGT 2700 ACTCAAAAGC GGTCGATGTC AGATGCTGGA CCGCCGCACG GTAGAAATGG CCTTCGCCTA 2760 CGCATTAGCA CTGTTCGCAG CAGCCCGACA AGAAGAGGCC GGCGCCCAAG TCTCCGTCCC 2820 ACGGGCCCTA GACCGCCAGG CCGCACTCTT ACAAATACAA GAATTTATGA TCACCTGCCT 2880 CTCACAAACA CCACCACGCA CCACGTTGCT GCTGTATCCC ACGGCCGTGG ACCTGGCCAA 2940 ACGAGCCCTT TGGACACCGA ATCAGATCAC CGACATCACC AGCCTCGTAC GCCTGGTCTA 3000 CATACTCTCT AAACAGAATC AGCAACATCT CATCCCCCAG TGGGCACTAC GACAGATCGC 3060 CGACTTTGCC CTAAAACTAC ACAAAACGCA CCTGGCCTCT TTTCTTTCAG CCTTCGCGCG 3120 TCAAGAACTC TACCTCATGG GCAGCCTCGT CCACTCCATG CTAGTACATA CGACGGAGAG 3180 ACGCGAAATC TTCATCGTAG AAACGGGCCT CTGTTCATTA GCCGAGCTAT CACACTTTAC 3240 GCAGTTGCTA GCTCATCCGC ACCACGAATA CCTCAGCGAC CTGTACACAC CCTGTTCCAG 3300 TAGCGGGCGA CGCGATCACT CGCTCGAACG CCTCACACGT CTCTTCCCCG ATGCCACCGT 3360 CCCCACTACC GTTCCCGCCG CCCTCTCCAT CCTATCTACC ATGCAACCAA GCACGCTAGA 3420 AACCTTCCCC GACCTGTTTT GTCTGCCGCT CGGCGAATCC TTCTCCGCGC TGACCGTCTC 3480 CGAACACGTC AGTTATGTCG TAACAAACCA GTACCTGATC AAAGGTATCT CCTACCCTGT 3540 CTCCACCACC GTCGTAGGCC AGAGCCTCAT CATCACCCAG ACGGACAGTC AAACTAAATG 3600 CGAACTGACG CGCAACATGC ATACCACACA CAGCATCACA GCGGCGCTCA ACATTTCCCT 3660 AGAAAACTGC GCCTTTTGCC AAAGCGCCCT ACTAGAATAC GACGACACGC AAGGCGTCAT 3720 CAACATCATG TACATGCACG ACTCGGACGA CGTCCTTTTC GCCCTGGATC CCTACAACGA 3780 AGTGGTGGTC TCATCTCCGC GAACTCACTA CCTCATGCTT TTGAAAAACG GTACGGTCCT 3840 AGAAGTAACT GACGTCGTCG TGGACGCTAC CGACAGTCGT CTCCTCATGA TGTCCGTCTA 3900 CGCGCTATCG GCCATCATCG GCATCTATCT GCTCTACCGC ATGCTCAAGA CATGCTGATT 3960 TTTATCTCGA GTCTAGAATC GATCCCGGGT TTTTATGACT AGTTAATCAC GGCCGCTTAT 4020 AAAGATCTAA AATGCATAAT TTCTAAATAA TGAAAAAAAA GTACATCATG AGCAACGCGT 4080 TAGTATATTT TACAATGGAG ATTAACGCTC TATACCGTTC TATGTTTATT GATTCAGATG 4140 ATGTTTTAGA AAAGAAAGTT ATTGAATATG AAAACTTTAA TGAAGATGAA GATGACGACG 4200 ATGATTATTG TTGTAAATCT GTTTTAGATG AAGAAGATGA CGCGCTAAAG TATACTATGG 4260 TTACAAAGTA TAAGTCTATA CTACTAATGG CGACTTGTGC AAGAAGGTAT AGTATAGTGA 4320 AAATGTTGTT AGATTATGAT TATGAAAAAC CAAATAAATC AGATCCATAT CTAAAGGTAT 4380 CTCCTTTGCA CATAATTTCA TCTATTCCTA GTTTAGAATA CCTGCAG 4427 2651 base pairs nucleic acid single linear DNA (genomic) unknown 13 AAGACTAATT TGTAAACCAT CTTACTCAAA ATATGTAACA ATAGTACGAT GCAATGAGTA 60 AGACAATAGG AAATCTATCT TATATACACA TAATTATTCT ATCAATTTTA CCAATTAGTT 120 AGTGTAATGT TATAAAAACT AATTAATCAC TCGAGATAAA AATCAGCATG TCTTGAGCAT 180 GCGGTAGAGC AGATAGATGC CGATGATGGC CGATAGCGCG TAGACGGACA TCATGAGGAG 240 ACGACTGTCG GTAGCGTCCA CGACGACGTC AGTTACTTCT AGGACCGTAC CGTTTTTCAA 300 AAGCATGAGG TAGTGAGTTC GCGGAGATGA GACCACCACT TCGTTGTAGG GATCCAGGGC 360 GAAAAGGACG TCGTCCGAGT CGTGCATGTA CATGATGTTG ATGACGCCTT GCGTGTCGTC 420 GTATTCTAGT AGGGCGCTTT GGCAAAAGGC GCAGTTTTCT AGGGAAATGT TGAGCGCCGC 480 TGTGATGCTG TGTGTGGTAT GCATGTTGCG CGTCAGTTCG CATTTAGTTT GACTGTCCGT 540 CTGGGTGATG ATGAGGCTCT GGCCTACGAC GGTGGTGGAG ACAGGGTAGG AGATACCTTT 600 GATCAGGTAC TGGTTTGTTA CGACATAACT GACGTGTTCG GAGACGGTCA GCGCGGAGAA 660 GGATTCGCCG AGCGGCAGAC AAAACAGGTC GGGGAAGGTT TCTAGCGTGC TTGGTTGCAT 720 GGTAGATAGG ATGGAGAGGG CGGCGGGAAC GGTAGTGGGG ACGGTGGCAT CGGGGAAGAG 780 ACGTGTGAGG CGTTCGAGCG AGTGATCGCG TCGCCCGCTA CTGGAACAGG GTGTGTACAG 840 GTCGCTGAGG TATTCGTGGT GCGGATGAGC TAGCAACTGC GTAAAGTGTG ATAGCTCGGC 900 TAATGAACAG AGGCCCGTTT CTACGATGAA GATTTCGCGT CTCTCCGTCG TATGTACTAG 960 CATGGAGTGG ACGAGGCTGC CCATGAGGTA GAGTTCTTGA CGCGCGAAGG CTGAAAGAAA 1020 AGAGGCCAGG TGCGTTTTGT GTAGTTTTAG GGCAAAGTCG GCGATCTGTC GTAGTGCCCA 1080 CTGGGGGATG AGATGTTGCT GATTCTGTTT AGAGAGTATG TAGACCAGGC GTACGAGGCT 1140 GGTGATGTCG GTGATCTGAT TCGGTGTCCA AAGGGCTCGT TTGGCCAGGT CCACGGCCGT 1200 GGGATACAGC AGCAACGTGG TGCGTGGTGG TGTTTGTGAG AGGCAGGTGA TCATAAATTC 1260 TTGTATTTGT AAGAGTGCGG CCTGGCGGTC TAGGGCCCGT GGGACGGAGA CTTGGGCGCC 1320 GGCCTCTTCT TGTCGGGCTG CTGCGAACAG TGCTAATGCG TAGGCGAAGG CCATTTCTAC 1380 CGTGCGGCGG TCCAGCATCT GACATCGACC GCTTTTGAGT ACATCCACGG CGTAACGGTG 1440 AAAGCTGTTA CGTAGTAGTG CGCTGAGGTC CAGGTAGTTG AAGTCAAGTG CGGCGTCAAG 1500 AAAGTCCGGG TCTTTGAGAT AAGAGTGACG GTTCAGTTGA TCTTTCTTAA CTAGCACCAG 1560 GAGCTCGTGT TTTTCAGTTT GTCGTAGTAT AAAGTTGTCG CGTTGATAGG GCGCTTTAAA 1620 GAGTACGCGT GGAAGATGGC CGAAGATAAG CAGCATGGGT GTGTCGTCGT CTATGGACAC 1680 CGTAACTACG AAGAAGTCCT CGGTCAGTGT TATTTTAACG TAACGTAGTT CGTCGATGAG 1740 GTAAAAGCCT TGGTGCAAAC AAGGTGTGAC GGTGCTGAAT AGTAGATCGT GTCCATCAAA 1800 GAGGATACAG GTCTGGTTAA AGTGTGGTCG GTGTAGTCCT GAGGTGGTAT GTGATTCTGT 1860 CCAGCCGTGT GGAGTGGTTT GCGGTGGCAT CCAAACGTGA GGTATTGACA GGTCAATGGG 1920 TGGTGGCACA GTGGTGGGCT GTTCACCTAG GCTGTCCTGT GCCTTTAGCT GCTGCGAAAA 1980 AGATCGGTAG CTGGCCAGGT CTTTGGATAC CAGCGCGTAA GTGTTAAGTC TCTGTTGGTA 2040 TCTTTCCAGG GTTTCGGTCA GATCTACCTG GTTCAGAAAC TGCTCCGCCA GAGGACCCGC 2100 AAAAAGACAT CGAGGCATAT GGAATACATA GTATTGATTA TAGCTTTGGA AAAAGTTGAA 2160 ACTGATGGCG TTTTCCCTGA CGACCGTGCT GTTACGGAGG CTGCTATTGT AGGTACACTG 2220 GGTGGTGTTT TCACGCAGGA AGCGGATGGG TCTCCCGTAG GTGTTGAGCA GTAGGTGAAA 2280 CGCTTTGTCC AGCGGTTCGG ATATGGCTTC TGCGCCATAT CGTGACGAAA GTAGGTGGCT 2340 GAGGAGACAG ACGGCGAGGA CGATGAGGTA GGAGGGGAGC CCGGGCCGCA TTTTATATTG 2400 TAATTATATA TTTTCAATTT TGAAATCCCA AAATATTATC ATATTCTTCC CAATAAACTC 2460 GAGCCCGGGG AATTCGGATC CTCGCGACTG CAGGGTACCT GAGTAGCTAA TTTTTAAACA 2520 AAAATGTGGG AGAATCTAAT TAGTTTTTCT TTACACAATT GACGTACATG AGTCTGAGTT 2580 CCTTGTTTTT GCTAATTATT TCATCCAATT TATTATTCTT GACGATATCG AGATCTTTTG 2640 TATAGGAGTC A 2651 1476 base pairs nucleic acid single linear DNA (genomic) unknown 14 ATGGAGTCCT CTGCCAAGAG AAAGATGGAC CCTGATAATC CTGACGAGGG CCCTTCCTCC 60 AAGGTGCCAC GGCCCGAGAC ACCCGTGACC AAGGCCACGA CGTTCCTGCA GACTATGTTG 120 AGGAAGGAGG TTAACAGTCA GCTGAGTCTG GGAGACCCGC TGTTTCCAGA GTTGGCCGAA 180 GAATCCCTCA AAACTTTTGA ACAAGTGACC GAGGATTGCA ACGAGAACCC CGAGAAAGAT 240 GTCCTGGCAG AACTCGTCAA ACAGATTAAG GTTCGAGTGG ACATGGTGCG GCATAGAATC 300 AAGGAGCACA TGCTGAAAAA ATATACCCAG ACGGAAGAGA AATTCACTGG CGCCTTTAAT 360 ATGATGGGAG GATGTTTGCA GAATGCCTTA GATATCTTAG ATAAGGTTCA TGAGCCTTTC 420 GAGGAGATGA AGTGTATTGG GCTAACTATG CAGAGCATGT ATGAGAACTA CATTGTACCT 480 GAGGATAAGC GGGAGATGTG GATGGCTTGT ATTAAGGAGC TGCATGATGT GAGCAAGGGC 540 GCCGCTAACA AGTTGGGGGG TGCACTGCAG GCTAAGGCCC GTGCTAAAAA GGATGAACTT 600 AGGAGAAAGA TGATGTATAT GTGCTACAGG AATATAGAGT TCTTTACCAA GAACTCAGCC 660 TTCCCTAAGA CCACCAATGG CTGCAGTCAG GCCATGGCGG CACTGCAGAA CTTGCCTCAG 720 TGCTCCCCTG ATGAGATTAT GGCTTATGCC CAGAAAATAT TTAAGATTTT GGATGAGGAG 780 AGAGACAAGG TGCTCACGCA CATTGATCAC ATATTTATGG ATATCCTCAC TACATGTGTG 840 GAAACAATGT GTAATGAGTA CAAGGTCACT AGTGACGCTT GTATGATGAC CATGTACGGG 900 GGCATCTCTC TCTTAAGTGA GTTCTGTCGG GTGCTGTGCT GCTATGTCTT AGAGGAGACT 960 AGTGTGATGC TGGCCAAGCG GCCTCTGATA ACCAAGCCTG AGGTTATCAG TGTAATGAAG 1020 CGCCGCATTG AGGAGATCTG CATGAAGGTC TTTGCCCAGT ACATTCTGGG GGCCGATCCT 1080 CTGAGAGTCT GCTCTCCTAG TGTGGATGAC CTACGGGCCA TCGCCGAGGA GTCAGATGAG 1140 GAAGAGGCTA TTGTAGCCTA CACTTTGGCC ACCGCTGGTG TCAGCTCCTC TGATTCTCTG 1200 GTGTCACCCC CAGAGTCCCC TGTACCCGCG ACTATCCCTC TGTCCTCAGT AATTGTGGCT 1260 GAGAACAGTG ATCAGGAAGA AAGTGAGCAG AGTGATGAGG AAGAGGAGGA GGGTGCTCAG 1320 GAGGAGCGGG AGGACACTGT GTCTGTCAAG TCTGAGCCAG TGTCTGAGAT AGAGGAAGTT 1380 GCCCCAGAGG AAGAGGAGGA TGGTGCTGAG GAACCCACCG CCTCTGGAGG TAAGAGTACC 1440 CACCCTATGG TGACTAGAAG CAAGGCTGAC CAGTAA 1476 1975 base pairs nucleic acid single linear DNA (genomic) unknown 15 ATATAATCCT CCACCAAAAT AGAGAATATA TATATCATCA TTTCATGATG TATACTACTG 60 ACATAGTTTC AATGTGAACT TTTCACTTTC TTGCCGGTTA TGAAGAATAT TTTTTATTTT 120 AATGGTCATT ACTAATCGTA TATTATAATT GAAAATGAAT TAGTTTAATA TGACGCTCGT 180 CATGGGATCC ATAAAAATTA CTGGTCAGCC TTGCTTCTAG TCACCATAGG GTGGGTACTC 240 TTACCTCCAG AGGCGGTGGG TTCCTCAGCA CCATCCTCCT CTTCCTCTGG GGCAACTTCC 300 TCTATCTCAG ACACTGGCTC AGACTTGACA GACACAGTGT CCTCCCGCTC CTCCTGAGCA 360 CCCTCCTCCT CTTCCTCATC ACTCTGCTCA CTTTCTTCCT GATCACTGTT CTCAGCCACA 420 ATTACTGAGG ACAGAGGGAT AGTCGCGGGT ACAGGGGACT CTGGGGGTGA CACCAGAGAA 480 TCAGAGGAGC TGACACCAGC GGTGGCCAAA GTGTAGGCTA CAATAGCCTC TTCCTCATCT 540 GACTCCTCGG CGATGGCCCG TAGGTCATCC ACACTAGGAG AGCAGACTCT CAGAGGATCG 600 GCCCCCAGAA TGTACTGGGC AAAGACCTTC ATGCAGATCT CCTCAATGCG GCGCTTCATT 660 ACACTGATAA CCTCAGGCTT GGTTATCAGA GGCCGCTTGG CCAGCATCAC ACTAGTCTCC 720 TCTAAGACAT AGCAGCACAG CACCCGACAG AACTCACTTA AGAGAGAGAT GCCCCCGTAC 780 ATGGTCATCA TACAAGCGTC ACTAGTGACC TTGTACTCAT TACACATTGT TTCCACACAT 840 GTAGTGAGGA TATCCATAAA TATGTGATCA ATGTGCGTGA GCACCTTGTC TCTCTCCTCA 900 TCCAAAATCT TAAATATTTT CTGGGCATAA GCCATAATCT CATCAGGGGA GCACTGAGGC 960 AAGTTCTGCA GTGCCGCCAT GGCCTGACTG CAGCCATTGG TGGTCTTAGG GAAGGCTGAG 1020 TTCTTGGTAA AGAACTCTAT ATTCCTGTAG CACATATACA TCATCTTTCT CCTAAGTTCA 1080 TCCTTTTTAG CACGGGCCTT AGCCTGCAGT GCACCCCCCA ACTTGTTAGC GGCGCCCTTG 1140 CTCACATCAT GCAGCTCCTT AATACAAGCC ATCCACATCT CCCGCTTATC CTCAGGTACA 1200 ATGTAGTTCT CATACATGCT CTGCATAGTT AGCCCAATAC ACTTCATCTC CTCGAAAGGC 1260 TCATGAACCT TATCTAAGAT ATCTAAGGCA TTCTGCAAAC ATCCTCCCAT CATATTAAAG 1320 GCGCCAGTGA ATTTCTCTTC CGTCTGGGTA TATTTTTTCA GCATGTGCTC CTTGATTCTA 1380 TGCCGCACCA TGTCCACTCG AACCTTAATC TGTTTGACGA GTTCTGCCAG GACATCTTTC 1440 TCGGGGTTCT CGTTGCAATC CTCGGTCACT TGTTCAAAAG TTTTGAGGGA TTCTTCGGCC 1500 AACTCTGGAA ACAGCGGGTC TCCCAGACTC AGCTGACTGT TAACCTCCTT CCTCAACATA 1560 GTCTGCAGGA ACGTCGTGGC CTTGGTCACG GGTGTCTCGG GCCGTGGCAC CTTGGAGGAA 1620 GGGCCCTCGT CAGGATTATC AGGGTCCATC TTTCTCTTGG CAGAGGACTC CATTACGATA 1680 CAAACTTAAC GGATATCGCG ATAATGAAAT AATTTATGAT TATTTCTCGC TTTCAATTTA 1740 ACACAACCCT CAAGAACCTT TGTATTTATT TTCACTTTTT AAGTATAGAA TAAAGAGATC 1800 CTGCTGTGGT AGATTCTGTG ACGCTAAGAA TAAGAATAAG AAGGAAGATG TAGAAGAGGG 1860 AAGAGAAGGA TGTTACAATT ATAAGAACCT TAATGATCTG GATGAATCCG AAGCACGTGT 1920 AGAATTTGGA CCATTATATA TGATAAATGA AGAAAAATCA GACATAAATA CATTG 1975 3499 base pairs nucleic acid single linear DNA (genomic) unknown 16 AAGCTTGCGG CCGCTCATTA GACAAGCGAA TGAGGGACGA AAACGTGGAG GAGGTATTAA 60 GTTTGGAGAA ATGGAGAGAG ACTGTTTAAT AGCGCATGGC GCAGCCAATA CTATTACAGA 120 AGTTTTGAAA GATTCGGAAG AAGATTATCA AGATGTGTAT GTTTGTGAAA ATTGTGGAGA 180 CATAGCAGCA CAAATCAAGG GTATTAATAC ATGTCTTAGA TGTTCAAAAC TTAATCTCTC 240 TCCTCTCTTA ACAAAAATTG ATACCACGCA CGTATCTAAA GTATTTCTTA CTCAAATGAA 300 CGCCAGAGGC GTAAAAGTCA AATTAGATTT CGAACGAAGG CCTCCTTCGT TTTATAAACC 360 ATTAGATAAA GTTGATCTCA AGCCGTCTTT TCTGGTGTAA TAAAAATTAA TTAATTACTC 420 GAGATAAAAA TTACTGGTCA GCCTTGCTTC TAGTCACCAT AGGGTGGGTA CTCTTACCTC 480 CAGAGGCGGT GGGTTCCTCA GCACCATCCT CCTCTTCCTC TGGGGCAACT TCCTCTATCT 540 CAGACACTGG CTCAGACTTG ACAGACACAG TGTCCTCCCG CTCCTCCTGA GCACCCTCCT 600 CCTCTTCCTC ATCACTCTGC TCACTTTCTT CCTGATCACT GTTCTCAGCC ACAATTACTG 660 AGGACAGAGG GATAGTCGCG GGTACAGGGG ACTCTGGGGG TGACACCAGA GAATCAGAGG 720 AGCTGACACC AGCGGTGGCC AAAGTGTAGG CTACAATAGC CTCTTCCTCA TCTGACTCCT 780 CGGCGATGGC CCGTAGGTCA TCCACACTAG GAGAGCAGAC TCTCAGAGGA TCGGCCCCCA 840 GAATGTACTG GGCAAAGACC TTCATGCAGA TCTCCTCAAT GCGGCGCTTC ATTACACTGA 900 TAACCTCAGG CTTGGTTATC AGAGGCCGCT TGGCCAGCAT CACACTAGTC TCCTCTAAGA 960 CATAGCAGCA CAGCACCCGA CAGAACTCAC TTAAGAGAGA GATGCCCCCG TACATGGTCA 1020 TCATACAAGC GTCACTAGTG ACCTTGTACT CATTACACAT TGTTTCCACA CATGTAGTGA 1080 GGATATCCAT AAATATGTGA TCAATGTGCG TGAGCACCTT GTCTCTCTCC TCATCCAAAA 1140 TCTTAAATAT TTTCTGGGCA TAAGCCATAA TCTCATCAGG GGAGCACTGA GGCAAGTTCT 1200 GCAGTGCCGC CATGGCCTGA CTGCAGCCAT TGGTGGTCTT AGGGAAGGCT GAGTTCTTGG 1260 TAAAGAACTC TATATTCCTG TAGCACATAT ACATCATCTT TCTCCTAAGT TCATCCTTTT 1320 TAGCACGGGC CTTAGCCTGC AGTGCACCCC CCAACTTGTT AGCGGCGCCC TTGCTCACAT 1380 CATGCAGCTC CTTAATACAA GCCATCCACA TCTCCCGCTT ATCCTCAGGT ACAATGTAGT 1440 TCTCATACAT GCTCTGCATA GTTAGCCCAA TACACTTCAT CTCCTCGAAA GGCTCATGAA 1500 CCTTATCTAA GATATCTAAG GCATTCTGCA AACATCCTCC CATCATATTA AAGGCGCCAG 1560 TGAATTTCTC TTCCGTCTGG GTATATTTTT TCAGCATGTG CTCCTTGATT CTATGCCGCA 1620 CCATGTCCAC TCGAACCTTA ATCTGTTTGA CGAGTTCTGC CAGGACATCT TTCTCGGGGT 1680 TCTCGTTGCA ATCCTCGGTC ACTTGTTCAA AAGTTTTGAG GGATTCTTCG GCCAACTCTG 1740 GAAACAGCGG GTCTCCCAGA CTCAGCTGAC TGTTAACCTC CTTCCTCAAC ATAGTCTGCA 1800 GGAACGTCGT GGCCTTGGTC ACGGGTGTCT CGGGCCGTGG CACCTTGGAG GAAGGGCCCT 1860 CGTCAGGATT ATCAGGGTCC ATCTTTCTCT TGGCAGAGGA CTCCATTACG ATACAAACTT 1920 AACGGATATC GCGATAATGA AATAATTTAT GATTATTTCT CGCTTTCAAT TTAACACAAC 1980 CCTCAAGAAC CTTTGTATTT ATTTTCACTT TTTAAGTATA GAATAAAGAA GCTCTAATTA 2040 ATTAAGCTAC AAATAGTTTC GTTTTCACCT TGTCTAATAA CTAATTAATT AACCCCGATA 2100 GCTGATTAGT TTTTGTTAAC AAAAATGTGG GAGAATCTAA TTAGTTTTTC TTTACACAAT 2160 TGACGTACAT GAGTCTGAGT TCCTTGTTTT TGCTAATTAT TTCATCCAAT TTATTATTCT 2220 TGACGATATC GAGATCTTTT GTATAGGAGT CAGACTTGTA TTCAACATGC TTTTCTATAA 2280 TCATCTTAGT TATTTCGGCA TCATCCAATA GTACATTTTC CAGATTAACA GAGTAGATAT 2340 TAATGTCGTA TTTGAACAGA GCCTGTAACA TCTCAATGTC TTTATTATCT ATAGCCAATT 2400 TAATGTCCGG AATGAAGAGA AGGGAATTAT TGGTGTTTGT CGACGTCATA TAGTCGAGCA 2460 AGAGAATCAT CATATCCACG TGTCCATTTT TTATAGTGGT GTGAATACAA CTAAGGAGAA 2520 TAGCCAGATC AAAAGTAGAT GGTATTTCTG AAAGAAAGTA TGATACAATA CTTACATCAT 2580 TAAGCATGAC GGCATGATAA AATGAAGTTT TCCATCCAGT TTTCCCATAG AACATCAGTC 2640 TCCAATTTTT CTTAAACAGT TTCACCGTTT GCATGTTACC ACTATCAACC GCATAATACA 2700 ATGCGGTGTT TCCTTTGTCA TCAAATTGTG AATCATCCAT TCCACTGAAT AGCAAAATCT 2760 TTACTATTTT GGTATCTTCT AATGTGGCTG CCTGATGTAA TGGAAATTCA TTCTCTAGAA 2820 GATTTTTCAA TGCTCCAGCG TTCAACAACG TACATACTAG ACGCACGTTA TTATCAGCTA 2880 TTGCATAATA CAAGGCACTA TGTCCATGGA CATCCGCCTT AAATGTATCT TTACTAGAGA 2940 GAAAGCTTTT CAGCTGCTTA GACTTCCAAG TATTAATTCG TGACAGATCC ATGTCTGAAA 3000 CGAGACGCTA ATTAGTGTAT ATTTTTTCAT TTTTTATAAT TTTGTCATAT TGCACCAGAA 3060 TTAATAATAT CTCTAATAGA TCTAATTTAA TTTAATTTAT ATAACTTATT TTTTGAATAT 3120 ACTTTTAATT AACAAAAGAG TTAAGTTACT CATATGGACG CCGTCCAGTC TGAACATCAA 3180 TCTTTTTAGC CAGAGATATC ATAGCCGCTC TTAGAGTTTC AGCGTGATTT TCCAACCTAA 3240 ATAGAACTTC ATCGTTGCGT TTACAACACT TTTCTATTTG TTCAAACTTT GTTGTTACAT 3300 TAGTAATCTT TTTTTCCAAA TTAGTTAGCC GTTGTTTGAG AGTTTCCTCA TTGTCGTCTT 3360 CATCGGCTTT AACAATTGCT TCGCGTTTAG CCTCCTGGCT GTTCTTATCA GCCTTTGTAG 3420 AAAAAAATTC AGTTGCTGGA ATTGCAAGAT CGTCATCTCC GGGGAAAAGA GTTCCGTCCA 3480 TTTAAAGCCG CGGGAATTC 3499 1386 base pairs nucleic acid single linear DNA (genomic) unknown 17 ATGGAGTCCT CTGCCAAGAG AAAGATGGAC CCTGATAATC CTGACGAGGG CCCTTCCTCC 60 AAGGTGCCAC GGCCCGAGAC ACCCGTGACC AAGGCCACGA CGTTCCTGCA GACTATGTTG 120 AGGAAGGAGG TTAACAGTCA GCTGAGTCTG GGAGACCCGC TGTTTCCAGA GTTGGCCGAA 180 GAATCCCTCA AAACTTTTGA ACAAGTGACC GAGGATTGCA ACGAGAACCC CGAGAAAGAT 240 GTCCTGGCAG AACTCGTCAA ACAGATTAAG GTTCGAGTGG ACATGGTGCG GCATAGAATC 300 AAGGAGCACA TGCTGAAAAA ATATACCCAG ACGGAAGAGA AATTCACTGG CGCCTTTAAT 360 ATGATGGGAG GATGTTTGCA GAATGCCTTA GATATCTTAG ATAAGGTTCA TGAGCCTTTC 420 GAGGAGATGA AGTGTATTGG GCTAACTATG CAGAGCATGT ATGAGAACTA CATTGTACCT 480 GAGGATAAGC GGGAGATGTG GATGGCTTGT ATTAAGGAGC TGCATGATGT GAGCAAGGGC 540 GCCGCTAACA AGTTGGGGGG TGCACTGCAG GCTAAGGCCC GTGCTAAAAA GGATGAACTT 600 AGGAGAAAGA TGATGTATAT GTGCTACAGG AATATAGAGT TCTTTACCAA GAACTCAGCC 660 TTCCCTAAGA CCACCAATGG CTGCAGTCAG GCCATGGCGG CACTGCAGAA CTTGCCTCAG 720 TGCTCCCCTG ATGAGATTAT GGCTTATGCC CAGAAAATAT TTAAGATTTT GGATGAGGAG 780 AGAGACAAGG TGCTCACGCA CATTGATCAC ATATTTATGG ATATCCTCAC TACATGTGTG 840 GAAACAATGT GTAATGAGTA CAAGGTCACT AGTGTGATGC TGGCCAAGCG GCCTCTGATA 900 ACCAAGCCTG AGGTTATCAG TGTAATGAAG CGCCGCATTG AGGAGATCTG CATGAAGGTC 960 TTTGCCCAGT ACATTCTGGG GGCCGATCCT CTGAGAGTCT GCTCTCCTAG TGTGGATGAC 1020 CTACGGGCCA TCGCCGAGGA GTCAGATGAG GAAGAGGCTA TTGTAGCCTA CACTTTGGCC 1080 ACCGCTGGTG TCAGCTCCTC TGATTCTCTG GTGTCACCCC CAGAGTCCCC TGTACCCGCG 1140 ACTATCCCTC TGTCCTCAGT AATTGTGGCT GAGAACAGTG ATCAGGAAGA AAGTGAGCAG 1200 AGTGATGAGG AAGAGGAGGA GGGTGCTCAG GAGGAGCGGG AGGACACTGT GTCTGTCAAG 1260 TCTGAGCCAG TGTCTGAGAT AGAGGAAGTT GCCCCAGAGG AAGAGGAGGA TGGTGCTGAG 1320 GAACCCACCG CCTCTGGAGG TAAGAGTACC CACCCTATGG TGACTAGAAG CAAGGCTGAC 1380 CAGTAA 1386 3409 base pairs nucleic acid single linear DNA (genomic) unknown 18 AAGCTTGCGG CCGCTCATTA GACAAGCGAA TGAGGGACGA AAACGTGGAG GAGGTATTAA 60 GTTTGGAGAA ATGGAGAGAG ACTGTTTAAT AGCGCATGGC GCAGCCAATA CTATTACAGA 120 AGTTTTGAAA GATTCGGAAG AAGATTATCA AGATGTGTAT GTTTGTGAAA ATTGTGGAGA 180 CATAGCAGCA CAAATCAAGG GTATTAATAC ATGTCTTAGA TGTTCAAAAC TTAATCTCTC 240 TCCTCTCTTA ACAAAAATTG ATACCACGCA CGTATCTAAA GTATTTCTTA CTCAAATGAA 300 CGCCAGAGGC GTAAAAGTCA AATTAGATTT CGAACGAAGG CCTCCTTCGT TTTATAAACC 360 ATTAGATAAA GTTGATCTCA AGCCGTCTTT TCTGGTGTAA TAAAAATTAA TTAATTACTC 420 GAGATAAAAA TTACTGGTCA GCCTTGCTTC TAGTCACCAT AGGGTGGGTA CTCTTACCTC 480 CAGAGGCGGT GGGTTCCTCA GCACCATCCT CCTCTTCCTC TGGGGCAACT TCCTCTATCT 540 CAGACACTGG CTCAGACTTG ACAGACACAG TGTCCTCCCG CTCCTCCTGA GCACCCTCCT 600 CCTCTTCCTC ATCACTCTGC TCACTTTCTT CCTGATCACT GTTCTCAGCC ACAATTACTG 660 AGGACAGAGG GATAGTCGCG GGTACAGGGG ACTCTGGGGG TGACACCAGA GAATCAGAGG 720 AGCTGACACC AGCGGTGGCC AAAGTGTAGG CTACAATAGC CTCTTCCTCA TCTGACTCCT 780 CGGCGATGGC CCGTAGGTCA TCCACACTAG GAGAGCAGAC TCTCAGAGGA TCGGCCCCCA 840 GAATGTACTG GGCAAAGACC TTCATGCAGA TCTCCTCAAT GCGGCGCTTC ATTACACTGA 900 TAACCTCAGG CTTGGTTATC AGAGGCCGCT TGGCCAGCAT CACACTAGTG ACCTTGTACT 960 CATTACACAT TGTTTCCACA CATGTAGTGA GGATATCCAT AAATATGTGA TCAATGTGCG 1020 TGAGCACCTT GTCTCTCTCC TCATCCAAAA TCTTAAATAT TTTCTGGGCA TAAGCCATAA 1080 TCTCATCAGG GGAGCACTGA GGCAAGTTCT GCAGTGCCGC CATGGCCTGA CTGCAGCCAT 1140 TGGTGGTCTT AGGGAAGGCT GAGTTCTTGG TAAAGAACTC TATATTCCTG TAGCACATAT 1200 ACATCATCTT TCTCCTAAGT TCATCCTTTT TAGCACGGGC CTTAGCCTGC AGTGCACCCC 1260 CCAACTTGTT AGCGGCGCCC TTGCTCACAT CATGCAGCTC CTTAATACAA GCCATCCACA 1320 TCTCCCGCTT ATCCTCAGGT ACAATGTAGT TCTCATACAT GCTCTGCATA GTTAGCCCAA 1380 TACACTTCAT CTCCTCGAAA GGCTCATGAA CCTTATCTAA GATATCTAAG GCATTCTGCA 1440 AACATCCTCC CATCATATTA AAGGCGCCAG TGAATTTCTC TTCCGTCTGG GTATATTTTT 1500 TCAGCATGTG CTCCTTGATT CTATGCCGCA CCATGTCCAC TCGAACCTTA ATCTGTTTGA 1560 CGAGTTCTGC CAGGACATCT TTCTCGGGGT TCTCGTTGCA ATCCTCGGTC ACTTGTTCAA 1620 AAGTTTTGAG GGATTCTTCG GCCAACTCTG GAAACAGCGG GTCTCCCAGA CTCAGCTGAC 1680 TGTTAACCTC CTTCCTCAAC ATAGTCTGCA GGAACGTCGT GGCCTTGGTC ACGGGTGTCT 1740 CGGGCCGTGG CACCTTGGAG GAAGGGCCCT CGTCAGGATT ATCAGGGTCC ATCTTTCTCT 1800 TGGCAGAGGA CTCCATTACG ATACAAACTT AACGGATATC GCGATAATGA AATAATTTAT 1860 GATTATTTCT CGCTTTCAAT TTAACACAAC CCTCAAGAAC CTTTGTATTT ATTTTCACTT 1920 TTTAAGTATA GAATAAAGAA GCTCTAATTA ATTAAGCTAC AAATAGTTTC GTTTTCACCT 1980 TGTCTAATAA CTAATTAATT AACCCCGATA GCTGATTAGT TTTTGTTAAC AAAAATGTGG 2040 GAGAATCTAA TTAGTTTTTC TTTACACAAT TGACGTACAT GAGTCTGAGT TCCTTGTTTT 2100 TGCTAATTAT TTCATCCAAT TTATTATTCT TGACGATATC GAGATCTTTT GTATAGGAGT 2160 CAGACTTGTA TTCAACATGC TTTTCTATAA TCATCTTAGT TATTTCGGCA TCATCCAATA 2220 GTACATTTTC CAGATTAACA GAGTAGATAT TAATGTCGTA TTTGAACAGA GCCTGTAACA 2280 TCTCAATGTC TTTATTATCT ATAGCCAATT TAATGTCCGG AATGAAGAGA AGGGAATTAT 2340 TGGTGTTTGT CGACGTCATA TAGTCGAGCA AGAGAATCAT CATATCCACG TGTCCATTTT 2400 TTATAGTGGT GTGAATACAA CTAAGGAGAA TAGCCAGATC AAAAGTAGAT GGTATTTCTG 2460 AAAGAAAGTA TGATACAATA CTTACATCAT TAAGCATGAC GGCATGATAA AATGAAGTTT 2520 TCCATCCAGT TTTCCCATAG AACATCAGTC TCCAATTTTT CTTAAACAGT TTCACCGTTT 2580 GCATGTTACC ACTATCAACC GCATAATACA ATGCGGTGTT TCCTTTGTCA TCAAATTGTG 2640 AATCATCCAT TCCACTGAAT AGCAAAATCT TTACTATTTT GGTATCTTCT AATGTGGCTG 2700 CCTGATGTAA TGGAAATTCA TTCTCTAGAA GATTTTTCAA TGCTCCAGCG TTCAACAACG 2760 TACATACTAG ACGCACGTTA TTATCAGCTA TTGCATAATA CAAGGCACTA TGTCCATGGA 2820 CATCCGCCTT AAATGTATCT TTACTAGAGA GAAAGCTTTT CAGCTGCTTA GACTTCCAAG 2880 TATTAATTCG TGACAGATCC ATGTCTGAAA CGAGACGCTA ATTAGTGTAT ATTTTTTCAT 2940 TTTTTATAAT TTTGTCATAT TGCACCAGAA TTAATAATAT CTCTAATAGA TCTAATTTAA 3000 TTTAATTTAT ATAACTTATT TTTTGAATAT ACTTTTAATT AACAAAAGAG TTAAGTTACT 3060 CATATGGACG CCGTCCAGTC TGAACATCAA TCTTTTTAGC CAGAGATATC ATAGCCGCTC 3120 TTAGAGTTTC AGCGTGATTT TCCAACCTAA ATAGAACTTC ATCGTTGCGT TTACAACACT 3180 TTTCTATTTG TTCAAACTTT GTTGTTACAT TAGTAATCTT TTTTTCCAAA TTAGTTAGCC 3240 GTTGTTTGAG AGTTTCCTCA TTGTCGTCTT CATCGGCTTT AACAATTGCT TCGCGTTTAG 3300 CCTCCTGGCT GTTCTTATCA GCCTTTGTAG AAAAAAATTC AGTTGCTGGA ATTGCAAGAT 3360 CGTCATCTCC GGGGAAAAGA GTTCCGTCCA TTTAAAGCCG CGGGAATTC 3409 1221 base pairs nucleic acid single linear DNA (genomic) unknown 19 ATGAAACAGA TTAAGGTTCG AGTGGACATG GTGCGGCATA GAATCAAGGA GCACATGCTG 60 AAAAAATATA CCCAGACGGA AGAGAAATTC ACTGGCGCCT TTAATATGAT GGGAGGATGT 120 TTGCAGAATG CCTTAGATAT CTTAGATAAG GTTCATGAGC CTTTCGAGGA GATGAAGTGT 180 ATTGGGCTAA CTATGCAGAG CATGTATGAG AACTACATTG TACCTGAGGA TAAGCGGGAG 240 ATGTGGATGG CTTGTATTAA GGAGCTGCAT GATGTGAGCA AGGGCGCCGC TAACAAGTTG 300 GGGGGTGCAC TGCAGGCTAA GGCCCGTGCT AAAAAGGATG AACTTAGGAG AAAGATGATG 360 TATATGTGCT ACAGGAATAT AGAGTTCTTT ACCAAGAACT CAGCCTTCCC TAAGACCACC 420 AATGGCTGCA GTCAGGCCAT GGCGGCACTG CAGAACTTGC CTCAGTGCTC CCCTGATGAG 480 ATTATGGCTT ATGCCCAGAA AATATTTAAG ATTTTGGATG AGGAGAGAGA CAAGGTGCTC 540 ACGCACATTG ATCACATATT TATGGATATC CTCACTACAT GTGTGGAAAC AATGTGTAAT 600 GAGTACAAGG TCACTAGTGA CGCTTGTATG ATGACCATGT ACGGGGGCAT CTCTCTCTTA 660 AGTGAGTTCT GTCGGGTGCT GTGCTGCTAT GTCTTAGAGG AGACTAGTGT GATGCTGGCC 720 AAGCGGCCTC TGATAACCAA GCCTGAGGTT ATCAGTGTAA TGAAGCGCCG CATTGAGGAG 780 ATCTGCATGA AGGTCTTTGC CCAGTACATT CTGGGGGCCG ATCCTCTGAG AGTCTGCTCT 840 CCTAGTGTGG ATGACCTACG GGCCATCGCC GAGGAGTCAG ATGAGGAAGA GGCTATTGTA 900 GCCTACACTT TGGCCACCGC TGGTGTCAGC TCCTCTGATT CTCTGGTGTC ACCCCCAGAG 960 TCCCCTGTAC CCGCGACTAT CCCTCTGTCC TCAGTAATTG TGGCTGAGAA CAGTGATCAG 1020 GAAGAAAGTG AGCAGAGTGA TGAGGAAGAG GAGGAGGGTG CTCAGGAGGA GCGGGAGGAC 1080 ACTGTGTCTG TCAAGTCTGA GCCAGTGTCT GAGATAGAGG AAGTTGCCCC AGAGGAAGAG 1140 GAGGATGGTG CTGAGGAACC CACCGCCTCT GGAGGTAAGA GTACCCACCC TATGGTGACT 1200 AGAAGCAAGG CTGACCAGTA A 1221 2577 base pairs nucleic acid single linear DNA (genomic) unknown 20 CTGCAGGTCG ACGGATCTGA GAATGGATGA TTCTCCAGCC GAAACATATT CTACCATGGC 60 TCCGTTTAAT TTGTTGATGA AGATGGATTC ATCCTTAAAT GTTTTCTCTG TAATAGTTTC 120 CACCGAAAGA CTATGCAAAG AATTTGGAAT GCGTTCCTTG TGCTTAATGT TTCCATAGAC 180 GGCTTCTAGA AGTTGATACA ACATAGGACT AGCCGCGGTA ACTTTTATTT TTAGAAAGTA 240 TCCATCGCTT CTATCTTGTT TAGATTTATT TTTATAAAGT TTAGTCTCTC CTTCCAACAT 300 AATAAAAGTG GAAGTCATTT GACTAGATAA ACTATCAGTA AGTTTTATAG AGATAGACGA 360 ACAATTAGCG TATTGAGAAG CATTTAGTGT AACGTATTCG ATACATTTTG CATTAGATTT 420 ACTAATCGAT TTTGCATACT CTATAACACC CGCACAAGTC TGTAGAGAAT CGCTAGATGC 480 AGTAGGTCTT GGTGAAGTTT CAACTCTCTT CTTGATTACC TTACTCATGA TTAAACCTAA 540 ATAATTGTAC TTTGTAATAT AATGATATAT ATTTTCACTT TATCTCATTT GAGAATAAAA 600 AGATCACAAA AATTAACTAA TCAGGATCCT TCTTTATTCT ATACTTAAAA AGTGAAAATA 660 AATACAAAGG TTCTTGAGGG TTGTGTTAAA TTGAAAGCGA GAAATAATCA TAAATTATTT 720 CATTATCGCG ATATCCGTTA AGTTTGTATC GTAATGAAAC AGATTAAGGT TCGAGTGGAC 780 ATGGTGCGGC ATAGAATCAA GGAGCACATG CTGAAAAAAT ATACCCAGAC GGAAGAGAAA 840 TTCACTGGCG CCTTTAATAT GATGGGAGGA TGTTTGCAGA ATGCCTTAGA TATCTTAGAT 900 AAGGTTCATG AGCCTTTCGA GGAGATGAAG TGTATTGGGC TAACTATGCA GAGCATGTAT 960 GAGAACTACA TTGTACCTGA GGATAAGCGG GAGATGTGGA TGGCTTGTAT TAAGGAGCTG 1020 CATGATGTGA GCAAGGGCGC CGCTAACAAG TTGGGGGGTG CACTGCAGGC TAAGGCCCGT 1080 GCTAAAAAGG ATGAACTTAG GAGAAAGATG ATGTATATGT GCTACAGGAA TATAGAGTTC 1140 TTTACCAAGA ACTCAGCCTT CCCTAAGACC ACCAATGGCT GCAGTCAGGC CATGGCGGCA 1200 CTGCAGAACT TGCCTCAGTG CTCCCCTGAT GAGATTATGG CTTATGCCCA GAAAATATTT 1260 AAGATTTTGG ATGAGGAGAG AGACAAGGTG CTCACGCACA TTGATCACAT ATTTATGGAT 1320 ATCCTCACTA CATGTGTGGA AACAATGTGT AATGAGTACA AGGTCACTAG TGACGCTTGT 1380 ATGATGACCA TGTACGGGGG CATCTCTCTC TTAAGTGAGT TCTGTCGGGT GCTGTGCTGC 1440 TATGTCTTAG AGGAGACTAG TGTGATGCTG GCCAAGCGGC CTCTGATAAC CAAGCCTGAG 1500 GTTATCAGTG TAATGAAGCG CCGCATTGAG GAGATCTGCA TGAAGGTCTT TGCCCAGTAC 1560 ATTCTGGGGG CCGATCCTCT GAGAGTCTGC TCTCCTAGTG TGGATGACCT ACGGGCCATC 1620 GCCGAGGAGT CAGATGAGGA AGAGGCTATT GTAGCCTACA CTTTGGCCAC CGCTGGTGTC 1680 AGCTCCTCTG ATTCTCTGGT GTCACCCCCA GAGTCCCCTG TACCCGCGAC TATCCCTCTG 1740 TCCTCAGTAA TTGTGGCTGA GAACAGTGAT CAGGAAGAAA GTGAGCAGAG TGATGAGGAA 1800 GAGGAGGAGG GTGCTCAGGA GGAGCGGGAG GACACTGTGT CTGTCAAGTC TGAGCCAGTG 1860 TCTGAGATAG AGGAAGTTGC CCCAGAGGAA GAGGAGGATG GTGCTGAGGA ACCCACCGCC 1920 TCTGGAGGTA AGAGTACCCA CCCTATGGTG ACTAGAAGCA AGGCTGACCA GTAATTTTTA 1980 TCTCGAGCCC GGGAGATCTT AGCTAACTGA TTTTTCTGGG AAAAAAATTA TTTAACTTTT 2040 CATTAATAGG GATTTGACGT ATGTAGCGTA CAAAATTATC GTTCCTGGTA TATAGATAAA 2100 GAGTCCTATA TATTTGAAAA TCGTTACGGC TCGATTAAAC TTTAATGATT GCATAGTGAA 2160 TATATCATTA GGATTTAACT CCTTGACTAT CATGGCGGCG CCAGAAATTA CCATCAAAAG 2220 CATTAATACA GTTATGCCGA TCGCAGTTAG AACGGTTATA GCATCCACCA TTTATATCTA 2280 AAAATTAGAT CAAAGAATAT GTGACAAAGT CCTAGTTGTA TACTGAGAAT TGACGAAACA 2340 ATGTTTCTTA CATATTTTTT TCTTATTAGT AACTGACTTA ATAGTAGGAA CTGGAAAGCT 2400 AGACTTGATT ATTCTATAAG TATAGATACC CTTCCAGATA ATGTTCTCTT TGATAAAAGT 2460 TCCAGAAAAT GTAGAATTTT TTAAAAAGTT ATCTTTTGCT ATTACCAAGA TTGTGTTTAG 2520 ACGCTTATTA TTAATATGAG TAATGAAATC CACACCGCCT CTAGATATGG GGAATTC 2577 3460 base pairs nucleic acid single linear DNA (genomic) unknown 21 GAATTGCGGC CGCTGAATGT TAAATGTTAT ACTTTGGATG AAGCTATAAA TATGCATTGG 60 AAAAATAATC CATTTAAAGA AAGGATTCAA ATACTACAAA ACCTAAGCGA TAATATGTTA 120 ACTAAGCTTA TTCTTAACGA CGCTTTAAAT ATACACAAAT AAACATAATT TTTGTATAAC 180 CTAACAAATA ACTAAAACAT AAAAATAATA AAAGGAAATG TAATATCGTA ATTATTTTAC 240 TCAGGAATGG GGTTAAATAT TTATATCACG TGTATATCTA TACTGTTATC GTATACTCTT 300 TACAATTACT ATTACGAATA TGCAAGAGAT AATAAGATTA CGTATTTAAG AGAATCTTGT 360 CATGATAATT GGGTACGACA TAGTGATAAA TGCTATTTCG CATCGTTACA TAAAGTCAGT 420 TGGAAAGATG GATTTGACAG ATGTAACTTA ATAGGTGCAA AAATGTTAAA TAACAGCATT 480 CTATCGGAAG ATAGGATACC AGTTATATTA TACAAAAATC ACTGGTTGGA TAAAACAGAT 540 TCTGCAATAT TCGTAAAAGA TGAAGATTAC TGCGAATTTG TAAACTATGA CAATAAAAAG 600 CCATTTATCT CAACGACATC GTGTAATTCT TCCATGTTTT ATGTATGTGT TTCAGATATT 660 ATGAGATTAC TATAAACTTT TTGTATACTT ATATTCCGTA AACTATATTA ATCATGAAGA 720 AAATGAAAAA GTATAGAAGC TGTTCACGAG CGGTTGTTGA AAACAACAAA ATTATACATT 780 CAAGATGGCT TACATATACG TCTGTGAGGC TATCATGGAT AATGACAATG CATCTCTAAA 840 TAGGTTTTTG GACAATGGAT TCGACCCTAA CACGGAATAT GGTACTCTAC AATCTCCTCT 900 TGAAATGGCT GTAATGTTCA AGAATACCGA GGCTATAAAA ATCTTGATGA GGTATGGAGC 960 TAAACCTGTA GTTACTGAAT GCACAACTTC TTGTCTGCAT GATGCGGTGT TGAGAGACGA 1020 CTACAAAATA GTGAAAGATC TGTTGAAGAA TAACTATGTA AACAATGTTC TTTACAGCGG 1080 AGGCTTTACT CCTTTGTGTT TGGCAGCTTA CCTTAACAAA GTTAATTTGG TTAAACTTCT 1140 ATTGGCTCAT TCGGCGGATG TAGATATTTC AAACACGGAT CGGTTAACTC CTCTACATAT 1200 AGCCGTATCA AATAAAAATT TAACAATGGT TAAACTTCTA TTGAACAAAG GTGCTGATAC 1260 TGACTTGCTG GATAACATGG GACGTACTCC TTTAATGATC GCTGTACAAT CTGGAAATAT 1320 TGAAATATGT AGCACACTAC TTAAAAAAAA TAAAATGTCC AGAACTGGGA AAAATTGATC 1380 TTGCCAGCTG TAATTCATGG TAGAAAAGAA GTGCTCAGGC TACTTTTCAA CAAAGGAGCA 1440 GATGTAAACT ACATCTTTGA AAGAAATGGA AAATCATATA CTGTTTTGGA ATTGATTAAA 1500 GAAAGTTACT CTGAGACACA AAAGAGGTAG CTGAAGTGGT ACTCTCAAAG GTACGTGACT 1560 AATTAGCTAT AAAAAGGATC CGGGTTAATT AATTAGTCAT CAGGCAGGGC GAGAACGAGA 1620 CTATCTGCTC GTTAATTAAT TAGAGCTTCT TTATTCTATA CTTAAAAAGT GAAAATAAAT 1680 ACAAAGGTTC TTGAGGGTTG TGTTAAATTG AAAGCGAGAA ATAATCATAA ATTATTTCAT 1740 TATCGCGATA TCCGTTAAGT TTGTATCGTA ATGAAACAGA TTAAGGTTCG AGTGGACATG 1800 GTGCGGCATA GAATCAAGGA GCACATGCTG AAAAAATATA CCCAGACGGA AGAGAAATTC 1860 ACTGGCGCCT TTAATATGAT GGGAGGATGT TTGCAGAATG CCTTAGATAT CTTAGATAAG 1920 GTTCATGAGC CTTTCGAGGA GATGAAGTGT ATTGGGCTAA CTATGCAGAG CATGTATGAG 1980 AACTACATTG TACCTGAGGA TAAGCGGGAG ATGTGGATGG CTTGTATTAA GGAGCTGCAT 2040 GATGTGAGCA AGGGCGCCGC TAACAAGTTG GGGGGTGCAC TGCAGGCTAA GGCCCGTGCT 2100 AAAAAGGATG AACTTAGGAG AAAGATGATG TATATGTGCT ACAGGAATAT AGAGTTCTTT 2160 ACCAAGAACT CAGCCTTCCC TAAGACCACC AATGGCTGCA GTCAGGCCAT GGCGGCACTG 2220 CAGAACTTGC CTCAGTGCTC CCCTGATGAG ATTATGGCTT ATGCCCAGAA AATATTTAAG 2280 ATTTTGGATG AGGAGAGAGA CAAGGTGCTC ACGCACATTG ATCACATATT TATGGATATC 2340 CTCACTACAT GTGTGGAAAC AATGTGTAAT GAGTACAAGG TCACTAGTGA CGCTTGTATG 2400 ATGACCATGT ACGGGGGCAT CTCTCTCTTA AGTGAGTTCT GTCGGGTGCT GTGCTGCTAT 2460 GTCTTAGAGG AGACTAGTGT GATGCTGGCC AAGCGGCCTC TGATAACCAA GCCTGAGGTT 2520 ATCAGTGTAA TGAAGCGCCG CATTGAGGAG ATCTGCATGA AGGTCTTTGC CCAGTACATT 2580 CTGGGGGCCG ATCCTCTGAG AGTCTGCTCT CCTAGTGTGG ATGACCTACG GGCCATCGCC 2640 GAGGAGTCAG ATGAGGAAGA GGCTATTGTA GCCTACACTT TGGCCACCGC TGGTGTCAGC 2700 TCCTCTGATT CTCTGGTGTC ACCCCCAGAG TCCCCTGTAC CCGCGACTAT CCCTCTGTCC 2760 TCAGTAATTG TGGCTGAGAA CAGTGATCAG GAAGAAAGTG AGCAGAGTGA TGAGGAAGAG 2820 GAGGAGGGTG CTCAGGAGGA GCGGGAGGAC ACTGTGTCTG TCAAGTCTGA GCCAGTGTCT 2880 GAGATAGAGG AAGTTGCCCC AGAGGAAGAG GAGGATGGTG CTGAGGAACC CACCGCCTCT 2940 GGAGGTAAGA GTACCCACCC TATGGTGACT AGAAGCAAGG CTGACCAGTA ATTTTTATCT 3000 CGAGTCTAGA ATCGATCCCG GGTTTTTATG ACTAGTTAAT CACGGCCGCT TATAAAGATC 3060 TAAAATGCAT AATTTCTAAA TAATGAAAAA AAAGTACATC ATGAGCAACG CGTTAGTATA 3120 TTTTACAATG GAGATTAACG CTCTATACCG TTCTATGTTT ATTGATTCAG ATGATGTTTT 3180 AGAAAAGAAA GTTATTGAAT ATGAAAACTT TAATGAAGAT GAAGATGACG ACGATGATTA 3240 TTGTTGTAAA TCTGTTTTAG ATGAAGAAGA TGACGCGCTA AAGTATACTA TGGTTACAAA 3300 GTATAAGTCT ATACTACTAA TGGCGACTTG TGCAAGAAGG TATAGTATAG TGAAAATGTT 3360 GTTAGATTAT GATTATGAAA AACCAAATAA ATCAGATCCA TATCTAAAGG TATCTCCTTT 3420 GCACATAATT TCATCTATTC CTAGTTTAGA ATACCTGCAG 3460 1383 base pairs nucleic acid single linear DNA (genomic) unknown 22 ATGACGACGT TCCTGCAGAC TATGTTGAGG AAGGAGGTTA ACAGTCAGCT GAGTCTGGGA 60 GACCCGCTGT TTCCAGAGTT GGCCGAAGAA TCCCTCAAAA CTTTTGAACA AGTGACCGAG 120 GATTGCAACG AGAACCCCGA GAAAGATGTC CTGGCAGAAC TCGTCAAACA GATTAAGGTT 180 CGAGTGGACA TGGTGCGGCA TAGAATCAAG GAGCACATGC TGAAAAAATA TACCCAGACG 240 GAAGAGAAAT TCACTGGCGC CTTTAATATG ATGGGAGGAT GTTTGCAGAA TGCCTTAGAT 300 ATCTTAGATA AGGTTCATGA GCCTTTCGAG GAGATGAAGT GTATTGGGCT AACTATGCAG 360 AGCATGTATG AGAACTACAT TGTACCTGAG GATAAGCGGG AGATGTGGAT GGCTTGTATT 420 AAGGAGCTGC ATGATGTGAG CAAGGGCGCC GCTAACAAGT TGGGGGGTGC ACTGCAGGCT 480 AAGGCCCGTG CTAAAAAGGA TGAACTTAGG AGAAAGATGA TGTATATGTG CTACAGGAAT 540 ATAGAGTTCT TTACCAAGAA CTCAGCCTTC CCTAAGACCA CCAATGGCTG CAGTCAGGCC 600 ATGGCGGCAC TGCAGAACTT GCCTCAGTGC TCCCCTGATG AGATTATGGC TTATGCCCAG 660 AAAATATTTA AGATTTTGGA TGAGGAGAGA GACAAGGTGC TCACGCACAT TGATCACATA 720 TTTATGGATA TCCTCACTAC ATGTGTGGAA ACAATGTGTA ATGAGTACAA GGTCACTAGT 780 GACGCTTGTA TGATGACCAT GTACGGGGGC ATCTCTCTCT TAAGTGAGTT CTGTCGGGTG 840 CTGTGCTGCT ATGTCTTAGA GGAGACTAGT GTGATGCTGG CCAAGCGGCC TCTGATAACC 900 AAGCCTGAGG TTATCAGTGT AATGAAGCGC CGCATTGAGG AGATCTGCAT GAAGGTCTTT 960 GCCCAGTACA TTCTGGGGGC CGATCCTCTG AGAGTCTGCT CTCCTAGTGT GGATGACCTA 1020 CGGGCCATCG CCGAGGAGTC AGATGAGGAA GAGGCTATTG TAGCCTACAC TTTGGCCACC 1080 GCTGGTGTCA GCTCCTCTGA TTCTCTGGTG TCACCCCCAG AGTCCCCTGT ACCCGCGACT 1140 ATCCCTCTGT CCTCAGTAAT TGTGGCTGAG AACAGTGATC AGGAAGAAAG TGAGCAGAGT 1200 GATGAGGAAG AGGAGGAGGG TGCTCAGGAG GAGCGGGAGG ACACTGTGTC TGTCAAGTCT 1260 GAGCCAGTGT CTGAGATAGA GGAAGTTGCC CCAGAGGAAG AGGAGGATGG TGCTGAGGAA 1320 CCCACCGCCT CTGGAGGTAA GAGTACCCAC CCTATGGTGA CTAGAAGCAA GGCTGACCAG 1380 TAA 1383 2739 base pairs nucleic acid single linear DNA (genomic) unknown 23 CTGCAGGTCG ACGGATCTGA GAATGGATGA TTCTCCAGCC GAAACATATT CTACCATGGC 60 TCCGTTTAAT TTGTTGATGA AGATGGATTC ATCCTTAAAT GTTTTCTCTG TAATAGTTTC 120 CACCGAAAGA CTATGCAAAG AATTTGGAAT GCGTTCCTTG TGCTTAATGT TTCCATAGAC 180 GGCTTCTAGA AGTTGATACA ACATAGGACT AGCCGCGGTA ACTTTTATTT TTAGAAAGTA 240 TCCATCGCTT CTATCTTGTT TAGATTTATT TTTATAAAGT TTAGTCTCTC CTTCCAACAT 300 AATAAAAGTG GAAGTCATTT GACTAGATAA ACTATCAGTA AGTTTTATAG AGATAGACGA 360 ACAATTAGCG TATTGAGAAG CATTTAGTGT AACGTATTCG ATACATTTTG CATTAGATTT 420 ACTAATCGAT TTTGCATACT CTATAACACC CGCACAAGTC TGTAGAGAAT CGCTAGATGC 480 AGTAGGTCTT GGTGAAGTTT CAACTCTCTT CTTGATTACC TTACTCATGA TTAAACCTAA 540 ATAATTGTAC TTTGTAATAT AATGATATAT ATTTTCACTT TATCTCATTT GAGAATAAAA 600 AGATCACAAA AATTAACTAA TCAGGATCCT TCTTTATTCT ATACTTAAAA AGTGAAAATA 660 AATACAAAGG TTCTTGAGGG TTGTGTTAAA TTGAAAGCGA GAAATAATCA TAAATTATTT 720 CATTATCGCG ATATCCGTTA AGTTTGTATC GTAATGACGA CGTTCCTGCA GACTATGTTG 780 AGGAAGGAGG TTAACAGTCA GCTGAGTCTG GGAGACCCGC TGTTTCCAGA GTTGGCCGAA 840 GAATCCCTCA AAACTTTTGA ACAAGTGACC GAGGATTGCA ACGAGAACCC CGAGAAAGAT 900 GTCCTGGCAG AACTCGTCAA ACAGATTAAG GTTCGAGTGG ACATGGTGCG GCATAGAATC 960 AAGGAGCACA TGCTGAAAAA ATATACCCAG ACGGAAGAGA AATTCACTGG CGCCTTTAAT 1020 ATGATGGGAG GATGTTTGCA GAATGCCTTA GATATCTTAG ATAAGGTTCA TGAGCCTTTC 1080 GAGGAGATGA AGTGTATTGG GCTAACTATG CAGAGCATGT ATGAGAACTA CATTGTACCT 1140 GAGGATAAGC GGGAGATGTG GATGGCTTGT ATTAAGGAGC TGCATGATGT GAGCAAGGGC 1200 GCCGCTAACA AGTTGGGGGG TGCACTGCAG GCTAAGGCCC GTGCTAAAAA GGATGAACTT 1260 AGGAGAAAGA TGATGTATAT GTGCTACAGG AATATAGAGT TCTTTACCAA GAACTCAGCC 1320 TTCCCTAAGA CCACCAATGG CTGCAGTCAG GCCATGGCGG CACTGCAGAA CTTGCCTCAG 1380 TGCTCCCCTG ATGAGATTAT GGCTTATGCC CAGAAAATAT TTAAGATTTT GGATGAGGAG 1440 AGAGACAAGG TGCTCACGCA CATTGATCAC ATATTTATGG ATATCCTCAC TACATGTGTG 1500 GAAACAATGT GTAATGAGTA CAAGGTCACT AGTGACGCTT GTATGATGAC CATGTACGGG 1560 GGCATCTCTC TCTTAAGTGA GTTCTGTCGG GTGCTGTGCT GCTATGTCTT AGAGGAGACT 1620 AGTGTGATGC TGGCCAAGCG GCCTCTGATA ACCAAGCCTG AGGTTATCAG TGTAATGAAG 1680 CGCCGCATTG AGGAGATCTG CATGAAGGTC TTTGCCCAGT ACATTCTGGG GGCCGATCCT 1740 CTGAGAGTCT GCTCTCCTAG TGTGGATGAC CTACGGGCCA TCGCCGAGGA GTCAGATGAG 1800 GAAGAGGCTA TTGTAGCCTA CACTTTGGCC ACCGCTGGTG TCAGCTCCTC TGATTCTCTG 1860 GTGTCACCCC CAGAGTCCCC TGTACCCGCG ACTATCCCTC TGTCCTCAGT AATTGTGGCT 1920 GAGAACAGTG ATCAGGAAGA AAGTGAGCAG AGTGATGAGG AAGAGGAGGA GGGTGCTCAG 1980 GAGGAGCGGG AGGACACTGT GTCTGTCAAG TCTGAGCCAG TGTCTGAGAT AGAGGAAGTT 2040 GCCCCAGAGG AAGAGGAGGA TGGTGCTGAG GAACCCACCG CCTCTGGAGG TAAGAGTACC 2100 CACCCTATGG TGACTAGAAG CAAGGCTGAC CAGTAATTTT TATCTCGAGC CCGGGAGATC 2160 TTAGCTAACT GATTTTTCTG GGAAAAAAAT TATTTAACTT TTCATTAATA GGGATTTGAC 2220 GTATGTAGCG TACAAAATTA TCGTTCCTGG TATATAGATA AAGAGTCCTA TATATTTGAA 2280 AATCGTTACG GCTCGATTAA ACTTTAATGA TTGCATAGTG AATATATCAT TAGGATTTAA 2340 CTCCTTGACT ATCATGGCGG CGCCAGAAAT TACCATCAAA AGCATTAATA CAGTTATGCC 2400 GATCGCAGTT AGAACGGTTA TAGCATCCAC CATTTATATC TAAAAATTAG ATCAAAGAAT 2460 ATGTGACAAA GTCCTAGTTG TATACTGAGA ATTGACGAAA CAATGTTTCT TACATATTTT 2520 TTTCTTATTA GTAACTGACT TAATAGTAGG AACTGGAAAG CTAGACTTGA TTATTCTATA 2580 AGTATAGATA CCCTTCCAGA TAATGTTCTC TTTGATAAAA GTTCCAGAAA ATGTAGAATT 2640 TTTTAAAAAG TTATCTTTTG CTATTACCAA GATTGTGTTT AGACGCTTAT TATTAATATG 2700 AGTAATGAAA TCCACACCGC CTCTAGATAT GGGGAATTC 2739 3622 base pairs nucleic acid single linear DNA (genomic) unknown 24 GAATTGCGGC CGCTGAATGT TAAATGTTAT ACTTTGGATG AAGCTATAAA TATGCATTGG 60 AAAAATAATC CATTTAAAGA AAGGATTCAA ATACTACAAA ACCTAAGCGA TAATATGTTA 120 ACTAAGCTTA TTCTTAACGA CGCTTTAAAT ATACACAAAT AAACATAATT TTTGTATAAC 180 CTAACAAATA ACTAAAACAT AAAAATAATA AAAGGAAATG TAATATCGTA ATTATTTTAC 240 TCAGGAATGG GGTTAAATAT TTATATCACG TGTATATCTA TACTGTTATC GTATACTCTT 300 TACAATTACT ATTACGAATA TGCAAGAGAT AATAAGATTA CGTATTTAAG AGAATCTTGT 360 CATGATAATT GGGTACGACA TAGTGATAAA TGCTATTTCG CATCGTTACA TAAAGTCAGT 420 TGGAAAGATG GATTTGACAG ATGTAACTTA ATAGGTGCAA AAATGTTAAA TAACAGCATT 480 CTATCGGAAG ATAGGATACC AGTTATATTA TACAAAAATC ACTGGTTGGA TAAAACAGAT 540 TCTGCAATAT TCGTAAAAGA TGAAGATTAC TGCGAATTTG TAAACTATGA CAATAAAAAG 600 CCATTTATCT CAACGACATC GTGTAATTCT TCCATGTTTT ATGTATGTGT TTCAGATATT 660 ATGAGATTAC TATAAACTTT TTGTATACTT ATATTCCGTA AACTATATTA ATCATGAAGA 720 AAATGAAAAA GTATAGAAGC TGTTCACGAG CGGTTGTTGA AAACAACAAA ATTATACATT 780 CAAGATGGCT TACATATACG TCTGTGAGGC TATCATGGAT AATGACAATG CATCTCTAAA 840 TAGGTTTTTG GACAATGGAT TCGACCCTAA CACGGAATAT GGTACTCTAC AATCTCCTCT 900 TGAAATGGCT GTAATGTTCA AGAATACCGA GGCTATAAAA ATCTTGATGA GGTATGGAGC 960 TAAACCTGTA GTTACTGAAT GCACAACTTC TTGTCTGCAT GATGCGGTGT TGAGAGACGA 1020 CTACAAAATA GTGAAAGATC TGTTGAAGAA TAACTATGTA AACAATGTTC TTTACAGCGG 1080 AGGCTTTACT CCTTTGTGTT TGGCAGCTTA CCTTAACAAA GTTAATTTGG TTAAACTTCT 1140 ATTGGCTCAT TCGGCGGATG TAGATATTTC AAACACGGAT CGGTTAACTC CTCTACATAT 1200 AGCCGTATCA AATAAAAATT TAACAATGGT TAAACTTCTA TTGAACAAAG GTGCTGATAC 1260 TGACTTGCTG GATAACATGG GACGTACTCC TTTAATGATC GCTGTACAAT CTGGAAATAT 1320 TGAAATATGT AGCACACTAC TTAAAAAAAA TAAAATGTCC AGAACTGGGA AAAATTGATC 1380 TTGCCAGCTG TAATTCATGG TAGAAAAGAA GTGCTCAGGC TACTTTTCAA CAAAGGAGCA 1440 GATGTAAACT ACATCTTTGA AAGAAATGGA AAATCATATA CTGTTTTGGA ATTGATTAAA 1500 GAAAGTTACT CTGAGACACA AAAGAGGTAG CTGAAGTGGT ACTCTCAAAG GTACGTGACT 1560 AATTAGCTAT AAAAAGGATC CGGGTTAATT AATTAGTCAT CAGGCAGGGC GAGAACGAGA 1620 CTATCTGCTC GTTAATTAAT TAGAGCTTCT TTATTCTATA CTTAAAAAGT GAAAATAAAT 1680 ACAAAGGTTC TTGAGGGTTG TGTTAAATTG AAAGCGAGAA ATAATCATAA ATTATTTCAT 1740 TATCGCGATA TCCGTTAAGT TTGTATCGTA ATGACGACGT TCCTGCAGAC TATGTTGAGG 1800 AAGGAGGTTA ACAGTCAGCT GAGTCTGGGA GACCCGCTGT TTCCAGAGTT GGCCGAAGAA 1860 TCCCTCAAAA CTTTTGAACA AGTGACCGAG GATTGCAACG AGAACCCCGA GAAAGATGTC 1920 CTGGCAGAAC TCGTCAAACA GATTAAGGTT CGAGTGGACA TGGTGCGGCA TAGAATCAAG 1980 GAGCACATGC TGAAAAAATA TACCCAGACG GAAGAGAAAT TCACTGGCGC CTTTAATATG 2040 ATGGGAGGAT GTTTGCAGAA TGCCTTAGAT ATCTTAGATA AGGTTCATGA GCCTTTCGAG 2100 GAGATGAAGT GTATTGGGCT AACTATGCAG AGCATGTATG AGAACTACAT TGTACCTGAG 2160 GATAAGCGGG AGATGTGGAT GGCTTGTATT AAGGAGCTGC ATGATGTGAG CAAGGGCGCC 2220 GCTAACAAGT TGGGGGGTGC ACTGCAGGCT AAGGCCCGTG CTAAAAAGGA TGAACTTAGG 2280 AGAAAGATGA TGTATATGTG CTACAGGAAT ATAGAGTTCT TTACCAAGAA CTCAGCCTTC 2340 CCTAAGACCA CCAATGGCTG CAGTCAGGCC ATGGCGGCAC TGCAGAACTT GCCTCAGTGC 2400 TCCCCTGATG AGATTATGGC TTATGCCCAG AAAATATTTA AGATTTTGGA TGAGGAGAGA 2460 GACAAGGTGC TCACGCACAT TGATCACATA TTTATGGATA TCCTCACTAC ATGTGTGGAA 2520 ACAATGTGTA ATGAGTACAA GGTCACTAGT GACGCTTGTA TGATGACCAT GTACGGGGGC 2580 ATCTCTCTCT TAAGTGAGTT CTGTCGGGTG CTGTGCTGCT ATGTCTTAGA GGAGACTAGT 2640 GTGATGCTGG CCAAGCGGCC TCTGATAACC AAGCCTGAGG TTATCAGTGT AATGAAGCGC 2700 CGCATTGAGG AGATCTGCAT GAAGGTCTTT GCCCAGTACA TTCTGGGGGC CGATCCTCTG 2760 AGAGTCTGCT CTCCTAGTGT GGATGACCTA CGGGCCATCG CCGAGGAGTC AGATGAGGAA 2820 GAGGCTATTG TAGCCTACAC TTTGGCCACC GCTGGTGTCA GCTCCTCTGA TTCTCTGGTG 2880 TCACCCCCAG AGTCCCCTGT ACCCGCGACT ATCCCTCTGT CCTCAGTAAT TGTGGCTGAG 2940 AACAGTGATC AGGAAGAAAG TGAGCAGAGT GATGAGGAAG AGGAGGAGGG TGCTCAGGAG 3000 GAGCGGGAGG ACACTGTGTC TGTCAAGTCT GAGCCAGTGT CTGAGATAGA GGAAGTTGCC 3060 CCAGAGGAAG AGGAGGATGG TGCTGAGGAA CCCACCGCCT CTGGAGGTAA GAGTACCCAC 3120 CCTATGGTGA CTAGAAGCAA GGCTGACCAG TAATTTTTAT CTCGAGTCTA GAATCGATCC 3180 CGGGTTTTTA TGACTAGTTA ATCACGGCCG CTTATAAAGA TCTAAAATGC ATAATTTCTA 3240 AATAATGAAA AAAAAGTACA TCATGAGCAA CGCGTTAGTA TATTTTACAA TGGAGATTAA 3300 CGCTCTATAC CGTTCTATGT TTATTGATTC AGATGATGTT TTAGAAAAGA AAGTTATTGA 3360 ATATGAAAAC TTTAATGAAG ATGAAGATGA CGACGATGAT TATTGTTGTA AATCTGTTTT 3420 AGATGAAGAA GATGACGCGC TAAAGTATAC TATGGTTACA AAGTATAAGT CTATACTACT 3480 AATGGCGACT TGTGCAAGAA GGTATAGTAT AGTGAAAATG TTGTTAGATT ATGATTATGA 3540 AAAACCAAAT AAATCAGATC CATATCTAAA GGTATCTCCT TTGCACATAA TTTCATCTAT 3600 TCCTAGTTTA GAATACCTGC AG 3622 1686 base pairs nucleic acid single linear DNA (genomic) unknown 25 ATGGAGTCGC GCGGTCGCCG TTGTCCCGAA ATGATATCCG TACTGGGTCC CATTTCGGGG 60 CACGTGCTGA AAGCCGTGTT TAGTCGCGGC GACACGCCGG TGCTGCCGCA CGAGACGCGA 120 CTCCTGCAGA CGGGTATCCA CGTGCGCGTG AGCCAGCCCT CGCTGATCCT GGTGTCGCAG 180 TACACGCCCG ACTCGACGCC ATGCCACCGC GGCGACAATC AGCTGCAGGT GCAGCACACG 240 TACTTTACGG GCAGCGAGGT GGAGAACGTG TCGGTCAACG TGCACAACCC CACGGGCCGG 300 AGCATCTGCC CCAGCCAAGA GCCCATGTCG ATCTATGTGT ACGCGCTGCC GCTCAAGATG 360 CTGAACATCC CCAGCATCAA CGTGCACCAC TACCCGTCGG CGGCCGAGCG CAAACACCGA 420 CACCTGCCCG TAGCTGACGC TGTGATTCAC GCGTCGGGCA AGCAGATGTG GCAGGCGCGT 480 CTCACGGTCT CGGGACTGGC CTGGACGCGT CAGCAGAACC AGTGGAAAGA GCCCGACGTC 540 TACTACACGT CAGCGTTCGT GTTTCCCACC AAGGACGTGG CACTGCGGCA CGTGGTGTGC 600 GCGCACGAGC TGGTTTGCTC CATGGAGAAC ACGCGCGCAA CCAAGATGCA GGTGATAGGT 660 GACCAGTACG TCAAGGTGTA CCTGGAGTCC TTCTGCGAGG ACGTGCCCTC CGGCAAGCTC 720 TTTATGCACG TCACGCTGGG CTCTGACGTG GAAGAGGACC TGACGATGAC CCGCAACCCG 780 CAACCCTTCA TGCGCCCCCA CGAGCGCAAC GGCTTTACGG TGTTGTGTCC CAAAAATATG 840 ATAATCAAAC CGGGCAAGAT CTCGCACATC ATGCTGGATG TGGCTTTTAC CTCACACGAG 900 CATTTTGGGC TGCTGTGTCC CAAGAGCATC CCGGGCCTGA GCATCTCAGG TAACCTATTG 960 ATGAACGGGC AGCAGATCTT CCTGGAGGTG CAAGCGATAC GCGAGACCGT GGAACTGCGT 1020 CAGTACGATC CCGTGGCTGC GCTCTTCTTT TTCGATATCG ACTTGCTGCT GCAGCGCGGG 1080 CCTCAGTACA GCGAACACCC CACCTTCACC AGCCAGTATC GCATCCAGGG CAAGCTTGAG 1140 TACCGACACA CCTGGGACCG GCACGACGAG GGTGCCGCCC AGGGCGACGA CGACGTCTGG 1200 ACCAGCGGAT CGGACTCCGA CGAGGAACTC GTAACCACCG AGCGCAAGAC GCCCCGCGTT 1260 ACCGGCGGCG GCGCCATGGC GGGCGCCTCC ACTTCCGCGG GCCGCAAACG CAAATCAGCA 1320 TCCTCGGCGA CGGCGTGCAC GGCGGGCGTT ATGACACGCG GCCGCCTTAA GGCCGAGTCC 1380 ACCGTCGCGC CCGAAGAGGA CACCGACGAG GATTCCGACA ACGAAATCCA CAATCCGGCC 1440 GTGTTCACCT GGCCGCCCTG GCAGGCCGGC ATCCTGGCCC GCAACCTGGT GCCCATGGTG 1500 GCTACGGTTC AGGGTCAGAA TCTGAAGTAC CAGGAGTTCT TCTGGGACGC CAACGACATC 1560 TACCGCATCT TCGCCGAATT GGAAGGCGTA TGGCAGCCCG CTGCGCAACC CAAACGTCGC 1620 CGCCACCGGC AAGACGCCTT GCCCGGGCCA TGCATCGCCT CGACGCCCAA AAAGCACCGA 1680 GGTTGA 1686 2745 base pairs nucleic acid single linear DNA (genomic) unknown 26 GTCGACGATT GTTCATGATG GCAAGATTTA TATATCTGGA GGTTACAACA ATAGTAGTGT 60 AGTTAATGTA ATATCGAATC TAGTCCTTAG CTATAATCCG ATATATGATG AATGGACCAA 120 ATTATCATCA TTAAACATTC CTAGAATTAA TCCCGCTCTA TGGTCAGCGC ATAATAAATT 180 ATATGTAGGA GGAGGAATAT CTGATGATGT TCGAACTAAT ACATCTGAAA CATACGATAA 240 AGAAAAAGAT TGTTGGACAT TGGATAATGG TCACGTGTTA CCACGCAATT ATATAATGTA 300 TAAATGCGAA CCGATTAAAC ATAAATATCC ATTGGAAAAA ACACAGTACA CGAATGATTT 360 TCTAAAGTAT TTGGAAAGTT TTATAGGTAG TTGATAGAAC AAAATACATA ATTTTGTAAA 420 AATAAATCAC TTTTTATACT AATATTTAAT TAATTAAGCT TGGTACCCTC GAAGCTTCTT 480 TATTCTATAC TTAAAAAGTG AAAATAAATA CAAAGGTTCT TGAGGGTTGT GTTAAATTGA 540 AAGCGAGAAA TAATCATAAA TTATTTCATT ATCGCGATAT CCGTTAAGTT TGTATCGTAA 600 TGGAGTCGCG CGGTCGCCGT TGTCCCGAAA TGATATCCGT ACTGGGTCCC ATTTCGGGGC 660 ACGTGCTGAA AGCCGTGTTT AGTCGCGGCG ACACGCCGGT GCTGCCGCAC GAGACGCGAC 720 TCCTGCAGAC GGGTATCCAC GTGCGCGTGA GCCAGCCCTC GCTGATCCTG GTGTCGCAGT 780 ACACGCCCGA CTCGACGCCA TGCCACCGCG GCGACAATCA GCTGCAGGTG CAGCACACGT 840 ACTTTACGGG CAGCGAGGTG GAGAACGTGT CGGTCAACGT GCACAACCCC ACGGGCCGGA 900 GCATCTGCCC CAGCCAAGAG CCCATGTCGA TCTATGTGTA CGCGCTGCCG CTCAAGATGC 960 TGAACATCCC CAGCATCAAC GTGCACCACT ACCCGTCGGC GGCCGAGCGC AAACACCGAC 1020 ACCTGCCCGT AGCTGACGCT GTGATTCACG CGTCGGGCAA GCAGATGTGG CAGGCGCGTC 1080 TCACGGTCTC GGGACTGGCC TGGACGCGTC AGCAGAACCA GTGGAAAGAG CCCGACGTCT 1140 ACTACACGTC AGCGTTCGTG TTTCCCACCA AGGACGTGGC ACTGCGGCAC GTGGTGTGCG 1200 CGCACGAGCT GGTTTGCTCC ATGGAGAACA CGCGCGCAAC CAAGATGCAG GTGATAGGTG 1260 ACCAGTACGT CAAGGTGTAC CTGGAGTCCT TCTGCGAGGA CGTGCCCTCC GGCAAGCTCT 1320 TTATGCACGT CACGCTGGGC TCTGACGTGG AAGAGGACCT GACGATGACC CGCAACCCGC 1380 AACCCTTCAT GCGCCCCCAC GAGCGCAACG GCTTTACGGT GTTGTGTCCC AAAAATATGA 1440 TAATCAAACC GGGCAAGATC TCGCACATCA TGCTGGATGT GGCTTTTACC TCACACGAGC 1500 ATTTTGGGCT GCTGTGTCCC AAGAGCATCC CGGGCCTGAG CATCTCAGGT AACCTATTGA 1560 TGAACGGGCA GCAGATCTTC CTGGAGGTGC AAGCGATACG CGAGACCGTG GAACTGCGTC 1620 AGTACGATCC CGTGGCTGCG CTCTTCTTTT TCGATATCGA CTTGCTGCTG CAGCGCGGGC 1680 CTCAGTACAG CGAACACCCC ACCTTCACCA GCCAGTATCG CATCCAGGGC AAGCTTGAGT 1740 ACCGACACAC CTGGGACCGG CACGACGAGG GTGCCGCCCA GGGCGACGAC GACGTCTGGA 1800 CCAGCGGATC GGACTCCGAC GAGGAACTCG TAACCACCGA GCGCAAGACG CCCCGCGTTA 1860 CCGGCGGCGG CGCCATGGCG GGCGCCTCCA CTTCCGCGGG CCGCAAACGC AAATCAGCAT 1920 CCTCGGCGAC GGCGTGCACG GCGGGCGTTA TGACACGCGG CCGCCTTAAG GCCGAGTCCA 1980 CCGTCGCGCC CGAAGAGGAC ACCGACGAGG ATTCCGACAA CGAAATCCAC AATCCGGCCG 2040 TGTTCACCTG GCCGCCCTGG CAGGCCGGCA TCCTGGCCCG CAACCTGGTG CCCATGGTGG 2100 CTACGGTTCA GGGTCAGAAT CTGAAGTACC AGGAGTTCTT CTGGGACGCC AACGACATCT 2160 ACCGCATCTT CGCCGAATTG GAAGGCGTAT GGCAGCCCGC TGCGCAACCC AAACGTCGCC 2220 GCCACCGGCA AGACGCCTTG CCCGGGCCAT GCATCGCCTC GACGCCCAAA AAGCACCGAG 2280 GTTGATTTTT ATGGATCCCC CGGGTAGCTA GCTAATTTTT CTTTTACGTA TTATATATGT 2340 AATAAACGTT CACGTAAATA CAAAACAGAG AACAAAGTCT AGATTTTTGA CTTACATAAA 2400 TGTCTGGGAT AGTAAAATCT ATCATATTGA GCGGACCATC TGGTTCAGGA AAGACAGCCA 2460 TAGCCAAAAG ACTATGGGAA TATATTTGGA TTTGTGGTGT CCCATACCAC TAGATTTCCT 2520 CGTCCTATGG AACGAGAAGG TGTCGATTAC CATTACGTTA ACAGAGAGGC CATCTGGAAG 2580 GGAATAGCCG CCGGAAACTT TCTAGAACAT ACTGAGTTTT TAGGAAATAT TTACGGAACT 2640 TCTAAAACTG CTGTGAATAC AGCGGCTATT AATAATCGTA TTTGTGTGAT GGATTTAAAC 2700 ATCGACGGTG TTAGAAGTTT TAAAAATACT TACCTGCAGA AGCTT 2745 3706 base pairs nucleic acid single linear DNA (genomic) unknown 27 AAGCTTCTAT CAAAAGTCTT AATGAGTTAG GTGTAGATAG TATAGATATT ACTACAAAGG 60 TATTCATATT TCCTATCAAT TCTAAAGTAG ATGATATTAA TAACTCAAAG ATGATGATAG 120 TAGATAATAG ATACGCTCAT ATAATGACTG CAAATTTGGA CGGTTCACAT TTTAATCATC 180 ACGCGTTCAT AAGTTTCAAC TGCATAGATC AAAATCTCAC TAAAAAGATA GCCGATGTAT 240 TTGAGAGAGA TTGGACATCT AACTACGCTA AAGAAATTAC AGTTATAAAT AATACATAAT 300 GGATTTTGTT ATCATCAGTT ATATTTAACA TAAGTACAAT AAAAAGTATT AAATAAAAAT 360 ACTTACTTAC GAAAAAATGT CATTATTACA AAAACTATAT TTTACAGAAC AATCTATAGT 420 AGAGTCCTTT AAGAGTTATA ATTTAAAAGA TAACCATAAT GTAATATTTA CCACATCAGA 480 TGTTGATACT GTTGTAGTAA TAAATGAAGA TAATGTACTG TTATCTACAA GATTATTATC 540 ATTTGATAAA ATTCTGTTTT TTAACTCCTT TAATAACGGT TTATCAAAAT ACGAAACTAT 600 TAGTGATACA ATATTAGATA TAGATACTCA TAATTATTAT ATACCTAGTT CTTCTTCTTT 660 GTTAGATATT CTAAAAAAAA GAGCGTGTGA TTTAGAATTA GAAGATCTAA ATTATGCGTT 720 AATAGGAGAC AATAGTAACT TATATTATAA AGATATGACT TACATGAATA ATTGGTTATT 780 TACTAAAGGA TTATTAGATT ACAAGTTTGT ATTATTGCGC GATGTAGATA AATGTTACAA 840 ACAGTATAAT AAAAAGAATA CTATAATAGA TATAATACAT CGCGATAACA GACAGTATAA 900 CATATGGGTT AAAAATGTTA TAGAATACTG TTCTCCTGGC TATATATTAT GGTTACATGA 960 TCTAAAAGCC GCTGCTGAAG ATGATTGGTT AAGATACGAT AACCGTATAA ACGAATTATC 1020 TGCGGATAAA TTATACACTT TCGAGTTCAT AGTTATATTA GAAAATAATA TAAAACATTT 1080 ACGAGTAGGT ACAATAATTG TACATCCAAA CAAGATAATA GCTAATGGTA CATCTAATAA 1140 TATACTTACT GATTTTCTAT CTTACGTAGA AGAACTAATA TATCATCATA ATTCATCTAT 1200 AATATTGGCC GGATATTTTT TAGAATTCTT TGAGACCACT ATTTTATCAG AATTTATTTC 1260 TTCATCTTCT GAATGGGTAA TGAATAGTAA CTGTTTAGTA CACCTGAAAA CAGGGTATGA 1320 AGCTATACTC TTTGATGCTA GTTTATTTTT CCAACTCTCT ACTAAAAGCA ATTATGTAAA 1380 ATATTGGACA AAGAAAACTT TGCAGTATAA GAACTTTTTT AAAGACGGTA AACAGTTAGC 1440 AAAATATATA ATTAAGAAAG ATAGTCAGGT GATAGATAGA GTATGTTATT TACACGCAGC 1500 TGTATATAAT CACGTAACTT ACTTAATGGA TACGTTTAAA ATTCCTGGTT TTGATTTTAA 1560 ATTCTCCGGA ATGATAGATA TACTACTGTT TGGAATATTG CATAAGGATA ATGAGAATAT 1620 ATTTTATCCG AAACGTGTTT CTGTAACTAA TATAATATCA GAATCTATCT ATGCAGATTT 1680 TTACTTTATA TCAGATGTTA ATAAATTCAG TAAAAAGATA GAATATAAAA CTATGTTTCC 1740 TATACTCGCA GAAAACTACT ATCCAAAAGG AAGGCCCTAT TTTACACATA CATCTAACGA 1800 AGATCTTCTG TCTATCTGTT TATGCGAAGT AACAGTTTGT AAAGATATAA AAAATCCATT 1860 ATTATATTCT AAAAAGGATA TATCAGCAAA ACGATTCATA GGTTTATTTA CATCTGTCGA 1920 TATAAATACG GCTGTTGAGT TAAGAGGATA TAAAATAAGA GTAATAGGAT GTTTAGAATG 1980 GCCTGAAAAG ATAAAAATAT TTAATTCTAA TCCTACATAC ATTAGATTAT TACTAACAGA 2040 AAGACGTTTA GATATTCTAC ATTCCTATCT GCTTAAATTT AATATAACAG AGGATATAGC 2100 TACCAGAGAT GGAGTCAGAA ATAATTTACC TATAATTTCT TTTATCGTCA GTTATTGTAG 2160 ATCGTATACT TATAAATTAC TAAATTGCCA TATGTACAAT TCGTGTAAGA TAACAAAGTG 2220 TAAATATAAT CAGGTAATAT ATAATCCTAT ATAGGAGTAT ATATAATTGA AAAAGTAAAA 2280 ATAAATCATA TAATAATGAA ACGAAATATC AGTAATAGAC AGGAACTGGC AGATTCTTCT 2340 TCTAATGAAG TAAGTACTGC TAAATCTCCA AAATTAGATA AAAATGATAC AGCAAATACA 2400 GCTTCATTCA ACGAATTACC TTTTAATTTT TTCAGACACA CCTTATTACA AACTAACTAA 2460 GTCAGATGAT GAGAAAGTAA ATATAAATTT AACTTATGGG TATAATATAA TAAAGATTCA 2520 TGATATTAAT AATTTACTTA ACGATGTTAA TAGACTTATT CCATCAACCC CTTCAAACCT 2580 TTCTGGATAT TATAAAATAC CAGTTAATGA TATTAAAATA GATTGTTTAA GAGATGTAAA 2640 TAATTATTTG GAGGTAAAGG ATATAAAATT AGTCTATCTT TCACATGGAA ATGAATTACC 2700 TAATATTAAT AATTATGATA GGAATTTTTT AGGATTTACA GCTGTTATAT GTATCAACAA 2760 TACAGGCAGA TCTATGGTTA TGGTAAAACA CTGTAACGGG AAGCAGCATT CTATGGTAAC 2820 TGGCCTATGT TTAATAGCCA GATCATTTTA CTCTATAAAC ATTTTACCAC AAATAATAGG 2880 ATCCTCTAGA TATTTAATAT TATATCTAAC AACAACAAAA AAATTTAACG ATGTATGGCC 2940 AGAAGTATTT TCTACTAATA AAGATAAAGA TAGTCTATCT TATCTACAAG ATATGAAAGA 3000 AGATAATCAT TTAGTAGTAG CTACTAATAT GGAAAGAAAT GTATACAAAA ACGTGGAAGC 3060 TTTTATATTA AATAGCATAT TACTAGAAGA TTTAAAATCT AGACTTAGTA TAACAAAACA 3120 GTTAAATGCC AATATCGATT CTATATTTCA TCATAACAGT AGTACATTAA TCAGTGATAT 3180 ACTGAAACGA TCTACAGACT CAACTATGCA AGGAATAAGC AATATGCCAA TTATGTCTAA 3240 TATTTTAACT TTAGAACTAA AACGATTCTA CCAATACTAA AAATAGGATA CGTGATAGGC 3300 TGTTAAAAGC TGCAATAAAT AGTAAGGATG TAGAAGAAAT ACTTTGTTCT ATACCTTCGG 3360 AGGAAAGAAC TTTAGAACAA CTTAAGTTTA ATCAAACTTG TATTTATGAA CACTATAAAA 3420 AAATTATGGA AGATACAAGT AAAAGAATGG ATGTTGAATG TCGTAGTTTA GAACATAACT 3480 ATACGGCTAA CTTATATAAA GTGTACGGAC AAAACGAATA TATGATTACT TATATACTAG 3540 CTCTCATAAG TAGGATTAAT AATATTATAG AAACTTTAAA ATATAATCTG GTGGGGCTAG 3600 ACGAATCTAC AATACGTAAT ATAAATTATA TAATTTCACA AAGAACAAAA AAAAATCAGT 3660 TTCTAATACC TTATAGATAA ACTATATTTT TTACCACTGA CAACAC 3706 3521 base pairs nucleic acid single linear DNA (genomic) unknown 28 GAGCTCGCGG CCGCCTATCA AAAGTCTTAA TGAGTTAGGT GTAGATAGTA TAGATATTAC 60 TACAAAGGTA TTCATATTTC CTATCAATTC TAAAGTAGAT GATATTAATA ACTCAAAGAT 120 GATGATAGTA GATAATAGAT ACGCTCATAT AATGACTGCA AATTTGGACG GTTCACATTT 180 TAATCATCAC GCGTTCATAA GTTTCAACTG CATAGATCAA AATCTCACTA AAAAGATAGC 240 CGATGTATTT GAGAGAGATT GGACATCTAA CTACGCTAAA GAAATTACAG TTATAAATAA 300 TACATAATGG ATTTTGTTAT CATCAGTTAT ATTTAACATA AGTACAATAA AAAGTATTAA 360 ATAAAAATAC TTACTTACGA AAAAATGACT AATTAGCTAT AAAAACCCAA CAAAAACTAA 420 TCAGCTATCG GGGTTAATTA ATTAGTTATT AGACAAGGTG AAAACGAAAC TATTTGTAGC 480 TTAATTAATT AGAGCTTCTT TATTCTATAC TTAAAAAGTG AAAATAAATA CAAAGGTTCT 540 TGAGGGTTGT GTTAAATTGA AAGCGAGAAA TAATCATAAA TTATTTCATT ATCGCGATAT 600 CCGTTAAGTT TGTATCGTAA TGGAGTCGCG CGGTCGCCGT TGTCCCGAAA TGATATCCGT 660 ACTGGGTCCC ATTTCGGGGC ACGTGCTGAA AGCCGTGTTT AGTCGCGGCG ACACGCCGGT 720 GCTGCCGCAC GAGACGCGAC TCCTGCAGAC GGGTATCCAC GTGCGCGTGA GCCAGCCCTC 780 GCTGATCCTG GTGTCGCAGT ACACGCCCGA CTCGACGCCA TGCCACCGCG GCGACAATCA 840 GCTGCAGGTG CAGCACACGT ACTTTACGGG CAGCGAGGTG GAGAACGTGT CGGTCAACGT 900 GCACAACCCC ACGGGCCGGA GCATCTGCCC CAGCCAAGAG CCCATGTCGA TCTATGTGTA 960 CGCGCTGCCG CTCAAGATGC TGAACATCCC CAGCATCAAC GTGCACCACT ACCCGTCGGC 1020 GGCCGAGCGC AAACACCGAC ACCTGCCCGT AGCTGACGCT GTGATTCACG CGTCGGGCAA 1080 GCAGATGTGG CAGGCGCGTC TCACGGTCTC GGGACTGGCC TGGACGCGTC AGCAGAACCA 1140 GTGGAAAGAG CCCGACGTCT ACTACACGTC AGCGTTCGTG TTTCCCACCA AGGACGTGGC 1200 ACTGCGGCAC GTGGTGTGCG CGCACGAGCT GGTTTGCTCC ATGGAGAACA CGCGCGCAAC 1260 CAAGATGCAG GTGATAGGTG ACCAGTACGT CAAGGTGTAC CTGGAGTCCT TCTGCGAGGA 1320 CGTGCCCTCC GGCAAGCTCT TTATGCACGT CACGCTGGGC TCTGACGTGG AAGAGGACCT 1380 GACGATGACC CGCAACCCGC AACCCTTCAT GCGCCCCCAC GAGCGCAACG GCTTTACGGT 1440 GTTGTGTCCC AAAAATATGA TAATCAAACC GGGCAAGATC TCGCACATCA TGCTGGATGT 1500 GGCTTTTACC TCACACGAGC ATTTTGGGCT GCTGTGTCCC AAGAGCATCC CGGGCCTGAG 1560 CATCTCAGGT AACCTATTGA TGAACGGGCA GCAGATCTTC CTGGAGGTGC AAGCGATACG 1620 CGAGACCGTG GAACTGCGTC AGTACGATCC CGTGGCTGCG CTCTTCTTTT TCGATATCGA 1680 CTTGCTGCTG CAGCGCGGGC CTCAGTACAG CGAACACCCC ACCTTCACCA GCCAGTATCG 1740 CATCCAGGGC AAGCTTGAGT ACCGACACAC CTGGGACCGG CACGACGAGG GTGCCGCCCA 1800 GGGCGACGAC GACGTCTGGA CCAGCGGATC GGACTCCGAC GAGGAACTCG TAACCACCGA 1860 GCGCAAGACG CCCCGCGTTA CCGGCGGCGG CGCCATGGCG GGCGCCTCCA CTTCCGCGGG 1920 CCGCAAACGC AAATCAGCAT CCTCGGCGAC GGCGTGCACG GCGGGCGTTA TGACACGCGG 1980 CCGCCTTAAG GCCGAGTCCA CCGTCGCGCC CGAAGAGGAC ACCGACGAGG ATTCCGACAA 2040 CGAAATCCAC AATCCGGCCG TGTTCACCTG GCCGCCCTGG CAGGCCGGCA TCCTGGCCCG 2100 CAACCTGGTG CCCATGGTGG CTACGGTTCA GGGTCAGAAT CTGAAGTACC AGGAGTTCTT 2160 CTGGGACGCC AACGACATCT ACCGCATCTT CGCCGAATTG GAAGGCGTAT GGCAGCCCGC 2220 TGCGCAACCC AAACGTCGCC GCCACCGGCA AGACGCCTTG CCCGGGCCAT GCATCGCCTC 2280 GACGCCCAAA AAGCACCGAG GTTGATTTTT ATGGATCCGG TACCCTCGAG GAATTCTTTT 2340 TATTGATTAA CTAGTCAAAT GAGTATATAT AATTGAAAAA GTAAAATATA AATCATATAA 2400 TAATGAAACG AAATATCAGT AATAGACAGG AACTGGCAGA TTCTTCTTCT AATGAAGTAA 2460 GTACTGCTAA ATCTCCAAAA TTAGATAAAA ATGATACAGC AAATACAGCT TCATTCAACG 2520 AATTACCTTT TAATTTTTTC AGACACACCT TATTACAAAC TAACTAAGTC AGATGATGAG 2580 AAAGTAAATA TAAATTTAAC TTATGGGTAT AATATAATAA AGATTCATGA TATTAATAAT 2640 TTACTTAACG ATGTTAATAG ACTTATTCCA TCAACCCCTT CAAACCTTTC TGGATATTAT 2700 AAAATACCAG TTAATGATAT TAAAATAGAT TGTTTAAGAG ATGTAAATAA TTATTTGGAG 2760 GTAAAGGATA TAAAATTAGT CTATCTTTCA CATGGAAATG AATTACCTAA TATTAATAAT 2820 TATGATAGGA ATTTTTTAGG ATTTACAGCT GTTATATGTA TCAACAATAC AGGCAGATCT 2880 ATGGTTATGG TAAAACACTG TAACGGGAAG CAGCATTCTA TGGTAACTGG CCTATGTTTA 2940 ATAGCCAGAT CATTTTACTC TATAAACATT TTACCACAAA TAATAGGATC CTCTAGATAT 3000 TTAATATTAT ATCTAACAAC AACAAAAAAA TTTAACGATG TATGGCCAGA AGTATTTTCT 3060 ACTAATAAAG ATAAAGATAG TCTATCTTAT CTACAAGATA TGAAAGAAGA TAATCATTTA 3120 GTAGTAGCTA CTAATATGGA AAGAAATGTA TACAAAAACG TGGAAGCTTT TATATTAAAT 3180 AGCATATTAC TAGAAGATTT AAAATCTAGA CTTAGTATAA CAAAACAGTT AAATGCCAAT 3240 ATCGATTCTA TATTTCATCA TAACAGTAGT ACATTAATCA GTGATATACT GAAACGATCT 3300 ACAGACTCAA CTATGCAAGG AATAAGCAAT ATGCCAATTA TGTCTAATAT TTTAACTTTA 3360 GAACTAAAAC GTTCTACCAA TACTAAAAAT AGGATACGTG ATAGGCTGTT AAAAGCTGCA 3420 ATAAATAGTA AGGATGTAGA AGAAATACTT TGTTCTATAC CTTCGGAGGA AAGAACTTTA 3480 GAACAACTTA AGTTTAATCA AACTTGTATT TATGAAGGTA C 3521 2160 base pairs nucleic acid single linear DNA (genomic) unknown 29 AAGACTAATT TGTAAACCAT CTTACTCAAA ATATGTAACA ATAGTACGAT GCAATGAGTA 60 AGACAATAGG AAATCTATCT TATATACACA TAATTATTCT ATCAATTTTA CCAATTAGTT 120 AGTGTAATGT TATAAAAACT AATTAATCAC TCGAGCCCCC TCGAAGCTTC TTTATTCTAT 180 ACTTAAAAAG TGAAAATAAA TACAAAGGTT CTTGAGGGTT GTGTTAAATT GAAAGCGAGA 240 AATAATCATA AATTATTTCA TTATCGCGAT ATCCGTTAAG TTTGTATCGT AATGGAGTCG 300 CGCGGTCGCC GTTGTCCCGA AATGATATCC GTACTGGGTC CCATTTCGGG GCACGTGCTG 360 AAAGCCGTGT TTAGTCGCGG CGACACGCCG GTGCTGCCGC ACGAGACGCG ACTCCTGCAG 420 ACGGGTATCC ACGTGCGCGT GAGCCAGCCC TCGCTGATCC TGGTGTCGCA GTACACGCCC 480 GACTCGACGC CATGCCACCG CGGCGACAAT CAGCTGCAGG TGCAGCACAC GTACTTTACG 540 GGCAGCGAGG TGGAGAACGT GTCGGTCAAC GTGCACAACC CCACGGGCCG GAGCATCTGC 600 CCCAGCCAAG AGCCCATGTC GATCTATGTG TACGCGCTGC CGCTCAAGAT GCTGAACATC 660 CCCAGCATCA ACGTGCACCA CTACCCGTCG GCGGCCGAGC GCAAACACCG ACACCTGCCC 720 GTAGCTGACG CTGTGATTCA CGCGTCGGGC AAGCAGATGT GGCAGGCGCG TCTCACGGTC 780 TCGGGACTGG CCTGGACGCG TCAGCAGAAC CAGTGGAAAG AGCCCGACGT CTACTACACG 840 TCAGCGTTCG TGTTTCCCAC CAAGGACGTG GCACTGCGGC ACGTGGTGTG CGCGCACGAG 900 CTGGTTTGCT CCATGGAGAA CACGCGCGCA ACCAAGATGC AGGTGATAGG TGACCAGTAC 960 GTCAAGGTGT ACCTGGAGTC CTTCTGCGAG GACGTGCCCT CCGGCAAGCT CTTTATGCAC 1020 GTCACGCTGG GCTCTGACGT GGAAGAGGAC CTGACGATGA CCCGCAACCC GCAACCCTTC 1080 ATGCGCCCCC ACGAGCGCAA CGGCTTTACG GTGTTGTGTC CCAAAAATAT GATAATCAAA 1140 CCGGGCAAGA TCTCGCACAT CATGCTGGAT GTGGCTTTTA CCTCACACGA GCATTTTGGG 1200 CTGCTGTGTC CCAAGAGCAT CCCGGGCCTG AGCATCTCAG GTAACCTATT GATGAACGGG 1260 CAGCAGATCT TCCTGGAGGT GCAAGCGATA CGCGAGACCG TGGAACTGCG TCAGTACGAT 1320 CCCGTGGCTG CGCTCTTCTT TTTCGATATC GACTTGCTGC TGCAGCGCGG GCCTCAGTAC 1380 AGCGAACACC CCACCTTCAC CAGCCAGTAT CGCATCCAGG GCAAGCTTGA GTACCGACAC 1440 ACCTGGGACC GGCACGACGA GGGTGCCGCC CAGGGCGACG ACGACGTCTG GACCAGCGGA 1500 TCGGACTCCG ACGAGGAACT CGTAACCACC GAGCGCAAGA CGCCCCGCGT TACCGGCGGC 1560 GGCGCCATGG CGGGCGCCTC CACTTCCGCG GGCCGCAAAC GCAAATCAGC ATCCTCGGCG 1620 ACGGCGTGCA CGGCGGGCGT TATGACACGC GGCCGCCTTA AGGCCGAGTC CACCGTCGCG 1680 CCCGAAGAGG ACACCGACGA GGATTCCGAC AACGAAATCC ACAATCCGGC CGTGTTCACC 1740 TGGCCGCCCT GGCAGGCCGG CATCCTGGCC CGCAACCTGG TGCCCATGGT GGCTACGGTT 1800 CAGGGTCAGA ATCTGAAGTA CCAGGAGTTC TTCTGGGACG CCAACGACAT CTACCGCATC 1860 TTCGCCGAAT TGGAAGGCGT ATGGCAGCCC GCTGCGCAAC CCAAACGTCG CCGCCACCGG 1920 CAAGACGCCT TGCCCGGGCC ATGCATCGCC TCGACGCCCA AAAAGCACCG AGGTTGATTT 1980 TTATGGATCC TCGCGACTGC AGGGTACCTG AGTAGCTAAT TTTTAAACAA AAATGTGGGA 2040 GAATCTAATT AGTTTTTCTT TACACAATTG ACGTACATGA GTCTGAGTTC CTTGTTTTTG 2100 CTAATTATTT CATCCAATTT ATTATTCTTG ACGATATCGA GATCTTTTGT ATAGGAGTCA 2160 3141 base pairs nucleic acid single linear DNA (genomic) unknown 30 ATGAGTTTGC AGTTTATCGG TCTACAGCGG CGCGATGTGG TGGCCCTGGT CAACTTTCTG 60 CGCCATCTCA CGCAAAAGCC CGACGTGGAT CTCGAGGCAC ACCCCAAGAT CCTGAAAAAA 120 TGTGGCGAAA AACGCCTGCA CCGGCGTACG GTGCTGTTCA ACGAGCTCAT GCTTTGGTTG 180 GGATACTACC GCGAGCTGCG TTTCCACAAC CCCGACCTCT CCTCGGTTCT CGAGGAGTTC 240 GAGGTGCGTT GCGCGGCCGT GGCGCGTCGC GGCTACACTT ACCCGTTCGG TGATCGTGGT 300 AAGGCGCGTG ACCACCTGGC TGTGCTAGAC CGTACCGAAT TCGATACGGA CGTACGCCAC 360 GATGCTGAGA TTGTGGAGCG CGCGCTCGTA AGCGCGGTCA TTCTGGCCAA GATGTCGGTG 420 CGCGAGACGC TGGTCACAGC CATCGGCCAG ACGGAACCCA TCGCTTTTGT GCACCTCAAG 480 GATACGGAGG TGCAGCGCAT TGAAGAAAAC CTGGAGGGTG TGCGCCGTAA CATGTTCTGC 540 GTGAAACCGC TCGACCTTAA CCTGGACCGG CACGCCAACA CGGCGCTGGT CAACGCCGTC 600 AACAAGCTCG TGTACACGGG CCGTCTCATC ATGAACGTGC GCAGGTCTTG GGAGGAGCTG 660 GAGCGCAAAT GTCTGGCGCG CATTCAGGAG CGCTGCAAGC TGCTGGTCAA GGAGCTGCGC 720 ATGTGCCTTT CCTTTGATTC CAACTACTGT CGCAATATCC TCAAACACGC CGTGGAAAAC 780 GGTGACTCGG CCGACACGCT GCTGGAGCTG CTCATCGAGG ACTTTGACAT CTACGTGGAC 840 AGCTTCCCGC AGTCGGCGCA CACCTTTTTG GGCGCGCGCC CGCCGTCGTT GGAGTTTGAC 900 GATGACGCCA ATCTCCTCTC GCTCGGCGGC GGTTCAGCCT TCTCGTCGGT ACCCAAGAAA 960 CATGTCCCCA CGCAGCCGCT GGACGGCTGG AGCTGGATCG CCAGTCCCTG GAAGGGACAC 1020 AAACCGTTCC GCTTCGAGGC CCATGGTTCT CTGGCACCGG CCGCCGACGC CCACGCCGCC 1080 CGTTCGGCGC GCGTCGGCTA TTACGACGAA GAGGAAAAGC GTCGCGAGCG GCAGAAACGG 1140 GTGGACGACG AGGTGGTGCA GCGTGAGAAA CAGCAGCTGA AGGCTTGGGA GGAGAGGCAG 1200 CAGAACCTGC AGCAACGTCA GCAGCAACCG CCGCCCCCGA CACGTAAACC GGGCGCCTCC 1260 CGGAGGCTCT TTGGCTCCAG TGCCGATGAG GACGACGACG ATGATGATGA CGAGAAAAAC 1320 ATCTTTACGC CCATCAAGAA ACCGGGAACT AGCGGCAAGG GCGCCGCTAG TGGCAACGGT 1380 GTTTCCAGCA TTTTCAGCGG CATGTTATCC TCGGGCAGTC AGAAACCGAC CAGCGGTCCC 1440 TTGAACATCC CGCAGCAACA ACAGCGTCAC GCGGCTTTCA GTCTCGTCTC CCCGCAGGTA 1500 ACCAAGGCCA GCCCGGGAAG GGTCCGTCGG GACAGCGCGT GGGACGTGAG GCCGCTCACG 1560 GAGACAAGAG GGGATCTTTT CTCGGGCGAC GAGGATTCCG ACAGCTCGGA TGGCTATCCC 1620 CCCAACCGTC AAGATCCGCG TTTCACCGAC ACGCTGGTGG ACATCACGGA TACCGAGACG 1680 AGCGCCAAAC CGCCCGTCAC CACCGCGTAC AAGTTCGAGC AACCGACGTT GACGTTCGGC 1740 GCCGGAGTTA ACGTCCCTGC TGGCGCCGGC GCTGCCATCC TCACGCCGAC GCCTGTCAAT 1800 CCTTCCACGG CCCCCGCTCC GGCCCCGACA CCTACCTTCG CGGGTACCCA AACCCCGGTC 1860 AACGGTAACT CGCCCTGGGC TCCGACGGCG CCGTTGCCCG GGGATATGAA CCCCGCCAAC 1920 TGGCCGCGCG AACGCGCGTG GGCCCTCAAG AATCCTCACC TGGCTTACAA TCCCTTCAGG 1980 ATGCCTACGA CTTCCACGAC TTCTCAAAAC AACGTGTCCA CCACCCCTCG GAGGCCGTCG 2040 ACTCCACGCG CCGCGGTGAC ACAAACAGCG TCTCAGAACG CCGCTGATGA GGTTTGGGCT 2100 TTAAGGGACC AAACTGCAGA GTCACCGGTC GAAGACAGCG AGGAGGAAGA CGACGACTCC 2160 TCGGACACCG GCTCCGTCGT CAGCCTGGGA CACACAACAC CGTCGTCCGA TTACAACGAC 2220 GTCATTTCGC CTCCCAGTCA GACGCCCGAG CAGTCGACGC CGTCCAGAAT ACGTAAAGCT 2280 AAGTTATCGT CTCCAATGAC GACGACATCC ACGAGCCAGA AACCGGTGCT GGGCAAGCGA 2340 GTCGCGACGC CGCACGCGTC CGCCCGAGCG CAGACGGTGA CGTCGACACC GGTTCAGGGA 2400 AGGGTAGAGA AACAGGTATC GGGCACGCCG TCGACGGTAC CCGCCACGCT GTTGCAACCT 2460 CAACCGGCTT CGTCTAAAAC AACGTCATCA AGGAACGTGA CTTCTGGCGC GAGAACCTCT 2520 TCCGCTTCGG CTCGACAGCC GTCAGCCTCG GCGTCCGTTT TGTCGCCCAC GGAGGATGAT 2580 GTCGTGTCCC CCGTCACGTC GCCGCTGTCC ATGCTTTCGT CAGCCTCTCC GTCCCCGGCC 2640 AAGAGTGCCC CTCCGTCTCC GGTGAAAGGT CGGGGCAGCC GCGTCGGTGT TCCTTCTTTG 2700 AAACCTACTT TGGGCGGCAA GGCGGTGGTA GGTCGACCGC CCTCGGTCCC CGTGAGCGGT 2760 AGCGCGCCGG GTCGCCTGTC CGGCACCAGC CGGGCCGCCT CGACCACGCC GACGTATCCC 2820 GCGGTAACCA CCGTTTACCC ACCGTCGTCT ACGGCCAAAA GCAGCGTATC GAATGCGCCG 2880 CCTGTGGCCT CCCCCTCCAT CCTGAAACCG GGGGCGAGCG CGGCTTTGCA ATCACGCCGC 2940 TCGACGGGGA CCGCCGCCGT AGGTTCCCCC GTCAAGAGCA CGACGGGCAT GAAAACGGTG 3000 GCTTTCGACC TATCGTCGCC CCAGAAGAGC GGTACGGGGC CGCAACCGGG TTCTGCCGGC 3060 ATGGGGGGCG CCAAAACGCC GTCGGACGCC GTGCAGAACA TCCTCCAAAA GATCGAGAAG 3120 ATTAAGAACA CGGAGGAATA G 3141 4075 base pairs nucleic acid single linear DNA (genomic) unknown 31 AAGCTTGCGG CCGCTCATTA GACAAGCGAA TGAGGGACGA AAACGTGGAG GAGGTATTAA 60 GTTTGGAGAA ATGGAGAGAG ACTGTTTAAT AGCGCATGGC GCAGCCAATA CTATTACAGA 120 AGTTTTGAAA GATTCGGAAG AAGATTATCA AGATGTGTAT GTTTGTGAAA ATTGTGGAGA 180 CATAGCAGCA CAAATCAAGG GTATTAATAC ATGTCTTAGA TGTTCAAAAC TTAATCTCTC 240 TCCTCTCTTA ACAAAAATTG ATACCACGCA CGTATCTAAA GTATTTCTTA CTCAAATGAA 300 CGCCAGAGGC GTAAAAGTCA AATTAGATTT CGAACGAAGG CCTCCTTCGT TTTATAAACC 360 ATTAGATAAA GTTGATCTCA AGCCGTCTTT TCTGGTGTAA TAAAAATTAA TTAATTACTC 420 GAGCCCCTAG CAATAAAAAC TATTCCTCCG TGTTCTTAAT CTTCTCGATC TTTTGGAGGA 480 TGTTCTGCAC GGCGTCCGAC GGCGTTTTGG CGCCCCCCAT GCCGGCAGAA CCCGGTTGCG 540 GCCCCGTACC GCTCTTCTGG GGCGACGATA GGTCGAAAGC CACCGTTTTC ATGCCCGTCG 600 TGCTCTTGAC GGGGGAACCT ACGGCGGCGG TCCCCGTCGA GCGGCGTGAT TGCAAAGCCG 660 CGCTCGCCCC CGGTTTCAGG ATGGAGGGGG AGGCCACAGG CGGCGCATTC GATACGCTGC 720 TTTTGGCCGT AGACGACGGT GGGTAAACGG TGGTTACCGC GGGATACGTC GGCGTGGTCG 780 AGGCGGCCCG GCTGGTGCCG GACAGGCGAC CCGGCGCGCT ACCGCTCACG GGTACCGAGG 840 GCGGTCGACC TACCACCGCC TTGCCGCCCA AAGTAGGTTT CAAAGAAGGA ACACCGACGC 900 GGCTGCCCCG ACCTTTCACC GGAGACGGAG GGGCACTCTT GGCCGGGGAC GGAGAGGCTG 960 ACGAAAGCAT GGACAGCGGC GACGTGACGG GGGACACGAC ATCATCCTCC GTGGGCGACA 1020 AAACGGACGC CGAGGCTGAC GGCTGTCGAG CCGAAGCGGA AGAGGTTCTC GCGCCAGAAG 1080 TCACGTTCCT TGATGACGTT GTTTTAGACG AAGCCGGTTG AGGTTGCAAC AGCGTGGCGG 1140 GTACCGTCGA CGGCGTGCCC GATACCTGTT TCTCTACCCT TCCCTGAACC GGTGTCGACG 1200 TCACCGTCTG CGCTCGGGCG GACGCGTGCG GCGTCGCGAC TCGCTTGCCC AGCACCGGTT 1260 TCTGGCTCGT GGATGTCGTC GTCATTGGAG ACGATAACTT AGCTTTACGT ATTCTGGACG 1320 GCGTCGACTG CTCGGGCGTC TGACTGGGAG GCGAAATGAC GTCGTTGTAA TCGGACGACG 1380 GTGTTGTGTG TCCCAGGCTG ACGACGGAGC CGGTGTCCGA GGAGTCGTCG TCTTCCTCCT 1440 CGCTGTCTTC GACCGGTGAC TCTGCAGTTT GGTCCCTTAA AGCCCAAACC TCATCAGCGG 1500 CGTTCTGAGA CGCTGTTTGT GTCACCGCGG CGCGTGGAGT CGACGGCCTC CGAGGGGTGG 1560 TGGACACGTT GTTTTGAGAA GTCGTGGAAG TCGTAGGCAT CCTGAAGGGA TTGTAAGCCA 1620 GGTGAGGATT CTTGAGGGCC CACGCGCGTT CGCGCGGCCA GTTGGCGGGG TTCATATCCC 1680 CGGGCAACGG CGCCGTCGGA GCCCAGGGCG AGTTACCGTT GACCGGGGTT TGGGTACCCG 1740 CGAAGGTAGG TGTCGGGGCC GGAGCGGGGG CCGTGGAAGG ATTGACAGGC GTCGGCGTGA 1800 GGATGGCAGC GCCGGCGCCA GCAGGGACGT TAACTCCGGC GCCGAACGTC AACGTCGGTT 1860 GCTCGAACTT GTACGCGGTG GTGACGGGCG GTTTGGCGCT CGTCTCGGTA TCCGTGATGT 1920 CCACCAGCGT GTCGGTGAAA CGCGGATCTT GACGGTTGGG GGGATAGCCA TCCGAGCTGT 1980 CGGAATCCTC GTCGCCCGAG AAAAGATCCC CTCTTGTCTC CGTGAGCGGC CTCACGTCCC 2040 ACGCGCTGTC CCGACGGACC CTTCCCGGGC TGGCCTTGGT TACCTGCGGG GAGACGAGAC 2100 TGAAAGCCGC GTGACGCTGT TGTTGCTGCG GGATGTTCAA GGGACCGCTG GTCGGTTTCT 2160 GACTGCCCGA GGATAACATG CCGCTGAAAA TGCTGGAAAC ACCGTTGCCA CTAGCGGCGC 2220 CCTTGCCGCT AGTTCCCGGT TTCTTGATGG GCGTAAAGAT GTTTTTCTCG TCATCATCAT 2280 CGTCGTCGTC CTCATCGGCA CTGGAGCCAA AGAGCCTCCG GGAGGCGCCC GGTTTACGTG 2340 TCGGGGGCGG CGGTTGCTGC TGACGTTGCT GCAGGTTCTG CTGCCTCTCC TCCCAAGCCT 2400 TCAGCTGCTG TTTCTCACGC TGCACCACCT CGTCGTCCAC CCGTTTCTGC CGCTCGCGAC 2460 GCTTTTCCTC TTCGTCGTAA TAGCCGACGC GCGCCGAACG GGCGGCGTGG GCGTCGGCGG 2520 CCGGTGCCAG AGAACCATGG GCCTCGAAGC GGAACGGTTT GTGTCCCTTC CAGGGACTGG 2580 CGATCCAGCT CCAGCCGTCC AGCGGCTGCG TGGGGACATG TTTCTTGGGT ACCGACGAGA 2640 AGGCTGAACC GCCGCCGAGC GAGAGGAGAT TGGCGTCATC GTCAAACTCC AACGACGGCG 2700 GGCGCGCGCC CAAAAAGGTG TGCGCCGACT GCGGGAAGCT GTCCACGTAG ATGTCAAAGT 2760 CCTCGATGAG CAGCTCCAGC AGCGTGTCGG CCGAGTCACC GTTTTCCACG GCGTGTTTGA 2820 GGATATTGCG ACAGTAGTTG GAATCAAAGG AAAGGCACAT GCGCAGCTCC TTGACCAGCA 2880 GCTTGCAGCG CTCCTGAATG CGCGCCAGAC ATTTGCGCTC CAGCTCCTCC CAAGACCTGC 2940 GCACGTTCAT GATGAGACGG CCCGTGTACA CGAGCTTGTT GACGGCGTTG ACCAGCGCCG 3000 TGTTGGCGTG CCGGTCCAGG TTAAGGTCGA GCGGTTTCAC GCAGAACATG TTACGGCGCA 3060 CACCCTCCAG GTTTTCTTCA ATGCGCTGCA CCTCCGTATC CTTGAGGTGC ACAAAAGCGA 3120 TGGGTTCCGT CTGGCCGATG GCTGTGACCA GCGTCTCGCG CACCGACATC TTGGCCAGAA 3180 TGACCGCGCT TACGAGCGCG CGCTCCACAA TCTCAGCATC GTGGCGTACG TCCGTATCGA 3240 ATTCGGTACG GTCTAGCACA GCCAGGTGGT CACGCGCCTT ACCACGATCA CCGAACGGGT 3300 AAGTGTAGCC GCGACGCGCC ACGGCCGCGC AACGCACCTC GAACTCCTCG AGAACCGAGG 3360 AGAGGTCGGG GTTGTGGAAA CGCAGCTCGC GGTAGTATCC CAACCAAAGC ATGAGCTCGT 3420 TGAACAGCAC CGTACGCCGG TGCAGGCGTT TTTCGCCACA TTTTTTCAGG ATCTTGGGGT 3480 GTGCCTCGAG ATCCACGTCG GGCTTTTGCG TGAGATGGCG CAGAAAGTTG ACCAGGGCCA 3540 CCACATCGCG CCGCTGTAGA CCGATAAACT GCAAACTCAT TTTATATTGT AATTATATAT 3600 TTTCAATTTT GAAATCCCAA AATATTATCA TATCTTCCCA ATAAAGCTAG GGGAGATCTA 3660 ATTTAATTTA ATTTATATAA CTTATTTTTT GAATATACTT TTAATTAACA AAAGAGTTAA 3720 GTTACTCATA TGGACGCCGT CCAGTCTGAA CATCAATCTT TTTAGCCAGA GATATCATAG 3780 CCGCTCTTAG AGTTTCAGCG TGATTTTCCA ACCTAAATAG AACTTCATCG TTGCGTTTAC 3840 AACACTTTTC TATTTGTTCA AACTTTGTTG TTACATTAGT AATCTTTTTT TCCAAATTAG 3900 TTAGCCGTTG TTTGAGAGTT TCCTCATTGT CGTCTTCATC GGCTTTAACA ATTGCTTCGC 3960 GTTTAGCCTC CTGGCTGTTC TTATCAGCCT TTGTAGAAAA AAATTCAGTT GCTGGAATTG 4020 CAAGATCGTC ATCTCCGGGG AAAAGAGTTC CGTCCATTTA AAGCCGCGGG AATTC 4075 4909 base pairs nucleic acid single linear DNA (genomic) unknown 32 GAGCTCGCGG CCGCCTATCA AAAGTCTTAA TGAGTTAGGT GTAGATAGTA TAGATATTAC 60 TACAAAGGTA TTCATATTTC CTATCAATTC TAAAGTAGAT GATATTAATA ACTCAAAGAT 120 GATGATAGTA GATAATAGAT ACGCTCATAT AATGACTGCA AATTTGGACG GTTCACATTT 180 TAATCATCAC GCGTTCATAA GTTTCAACTG CATAGATCAA AATCTCACTA AAAAGATAGC 240 CGATGTATTT GAGAGAGATT GGACATCTAA CTACGCTAAA GAAATTACAG TTATAAATAA 300 TACATAATGG ATTTTGTTAT CATCAGTTAT ATTTAACATA AGTACAATAA AAAGTATTAA 360 ATAAAAATAC TTACTTACGA AAAAATGACT AATTAGCTAT AAAAACCCGG GGGATCCTTA 420 ATTAATTAGT TATTAGACAA GGTGAAAACG AAACTATTTG TAGCTTAATT AATTAGCTGC 480 AGGGCTGCAG GAATTCTAGC AATAAAAACT ATTCCTCCGT GTTCTTAATC TTCTCGATCT 540 TTTGGAGGAT GTTCTGCACG GCGTCCGACG GCGTTTTGGC GCCCCCCATG CCGGCAGAAC 600 CCGGTTGCGG CCCCGTACCG CTCTTCTGGG GCGACGATAG GTCGAAAGCC ACCGTTTTCA 660 TGCCCGTCGT GCTCTTGACG GGGGAACCTA CGGCGGCGGT CCCCGTCGAG CGGCGTGATT 720 GCAAAGCCGC GCTCGCCCCC GGTTTCAGGA TGGAGGGGGA GGCCACAGGC GGCGCATTCG 780 ATACGCTGCT TTTGGCCGTA GACGACGGTG GGTAAACGGT GGTTACCGCG GGATACGTCG 840 GCGTGGTCGA GGCGGCCCGG CTGGTGCCGG ACAGGCGACC CGGCGCGCTA CCGCTCACGG 900 GTACCGAGGG CGGTCGACCT ACCACCGCCT TGCCGCCCAA AGTAGGTTTC AAAGAAGGAA 960 CACCGACGCG GCTGCCCCGA CCTTTCACCG GAGACGGAGG GGCACTCTTG GCCGGGGACG 1020 GAGAGGCTGA CGAAAGCATG GACAGCGGCG ACGTGACGGG GGACACGACA TCATCCTCCG 1080 TGGGCGACAA AACGGACGCC GAGGCTGACG GCTGTCGAGC CGAAGCGGAA GAGGTTCTCG 1140 CGCCAGAAGT CACGTTCCTT GATGACGTTG TTTTAGACGA AGCCGGTTGA GGTTGCAACA 1200 GCGTGGCGGG TACCGTCGAC GGCGTGCCCG ATACCTGTTT CTCTACCCTT CCCTGAACCG 1260 GTGTCGACGT CACCGTCTGC GCTCGGGCGG ACGCGTGCGG CGTCGCGACT CGCTTGCCCA 1320 GCACCGGTTT CTGGCTCGTG GATGTCGTCG TCATTGGAGA CGATAACTTA GCTTTACGTA 1380 TTCTGGACGG CGTCGACTGC TCGGGCGTCT GACTGGGAGG CGAAATGACG TCGTTGTAAT 1440 CGGACGACGG TGTTGTGTGT CCCAGGCTGA CGACGGAGCC GGTGTCCGAG GAGTCGTCGT 1500 CTTCCTCCTC GCTGTCTTCG ACCGGTGACT CTGCAGTTTG GTCCCTTAAA GCCCAAACCT 1560 CATCAGCGGC GTTCTGAGAC GCTGTTTGTG TCACCGCGGC GCGTGGAGTC GACGGCCTCC 1620 GAGGGGTGGT GGACACGTTG TTTTGAGAAG TCGTGGAAGT CGTAGGCATC CTGAAGGGAT 1680 TGTAAGCCAG GTGAGGATTC TTGAGGGCCC ACGCGCGTTC GCGCGGCCAG TTGGCGGGGT 1740 TCATATCCCC GGGCAACGGC GCCGTCGGAG CCCAGGGCGA GTTACCGTTG ACCGGGGTTT 1800 GGGTACCCGC GAAGGTAGGT GTCGGGGCCG GAGCGGGGGC CGTGGAAGGA TTGACAGGCG 1860 TCGGCGTGAG GATGGCAGCG CCGGCGCCAG CAGGGACGTT AACTCCGGCG CCGAACGTCA 1920 ACGTCGGTTG CTCGAACTTG TACGCGGTGG TGACGGGCGG TTTGGCGCTC GTCTCGGTAT 1980 CCGTGATGTC CACCAGCGTG TCGGTGAAAC GCGGATCTTG ACGGTTGGGG GGATAGCCAT 2040 CCGAGCTGTC GGAATCCTCG TCGCCCGAGA AAAGATCCCC TCTTGTCTCC GTGAGCGGCC 2100 TCACGTCCCA CGCGCTGTCC CGACGGACCC TTCCCGGGCT GGCCTTGGTT ACCTGCGGGG 2160 AGACGAGACT GAAAGCCGCG TGACGCTGTT GTTGCTGCGG GATGTTCAAG GGACCGCTGG 2220 TCGGTTTCTG ACTGCCCGAG GATAACATGC CGCTGAAAAT GCTGGAAACA CCGTTGCCAC 2280 TAGCGGCGCC CTTGCCGCTA GTTCCCGGTT TCTTGATGGG CGTAAAGATG TTTTTCTCGT 2340 CATCATCATC GTCGTCGTCC TCATCGGCAC TGGAGCCAAA GAGCCTCCGG GAGGCGCCCG 2400 GTTTACGTGT CGGGGGCGGC GGTTGCTGCT GACGTTGCTG CAGGTTCTGC TGCCTCTCCT 2460 CCCAAGCCTT CAGCTGCTGT TTCTCACGCT GCACCACCTC GTCGTCCACC CGTTTCTGCC 2520 GCTCGCGACG CTTTTCCTCT TCGTCGTAAT AGCCGACGCG CGCCGAACGG GCGGCGTGGG 2580 CGTCGGCGGC CGGTGCCAGA GAACCATGGG CCTCGAAGCG GAACGGTTTG TGTCCCTTCC 2640 AGGGACTGGC GATCCAGCTC CAGCCGTCCA GCGGCTGCGT GGGGACATGT TTCTTGGGTA 2700 CCGACGAGAA GGCTGAACCG CCGCCGAGCG AGAGGAGATT GGCGTCATCG TCAAACTCCA 2760 ACGACGGCGG GCGCGCGCCC AAAAAGGTGT GCGCCGACTG CGGGAAGCTG TCCACGTAGA 2820 TGTCAAAGTC CTCGATGAGC AGCTCCAGCA GCGTGTCGGC CGAGTCACCG TTTTCCACGG 2880 CGTGTTTGAG GATATTGCGA CAGTAGTTGG AATCAAAGGA AAGGCACATG CGCAGCTCCT 2940 TGACCAGCAG CTTGCAGCGC TCCTGAATGC GCGCCAGACA TTTGCGCTCC AGCTCCTCCC 3000 AAGACCTGCG CACGTTCATG ATGAGACGGC CCGTGTACAC GAGCTTGTTG ACGGCGTTGA 3060 CCAGCGCCGT GTTGGCGTGC CGGTCCAGGT TAAGGTCGAG CGGTTTCACG CAGAACATGT 3120 TACGGCGCAC ACCCTCCAGG TTTTCTTCAA TGCGCTGCAC CTCCGTATCC TTGAGGTGCA 3180 CAAAAGCGAT GGGTTCCGTC TGGCCGATGG CTGTGACCAG CGTCTCGCGC ACCGACATCT 3240 TGGCCAGAAT GACCGCGCTT ACGAGCGCGC GCTCCACAAT CTCAGCATCG TGGCGTACGT 3300 CCGTATCGAA TTCGGTACGG TCTAGCACAG CCAGGTGGTC ACGCGCCTTA CCACGATCAC 3360 CGAACGGGTA AGTGTAGCCG CGACGCGCCA CGGCCGCGCA ACGCACCTCG AACTCCTCGA 3420 GAACCGAGGA GAGGTCGGGG TTGTGGAAAC GCAGCTCGCG GTAGTATCCC AACCAAAGCA 3480 TGAGCTCGTT GAACAGCACC GTACGCCGGT GCAGGCGTTT TTCGCCACAT TTTTTCAGGA 3540 TCTTGGGGTG TGCCTCGAGA TCCACGTCGG GCTTTTGCGT GAGATGGCGC AGAAAGTTGA 3600 CCAGGGCCAC CACATCGCGC CGCTGTAGAC CGATAAACTG CAAACTCATT TTATATTGTA 3660 ATTATATATT TTCAATTTTG AAATCCCAAA ATATTATCAT ATCTTCCCAA TAAAGCTAGA 3720 TTCTTTTTAT TGATTAACTA GTCAAATGAG TATATATAAT TGAAAAAGTA AAATATAAAT 3780 CATATAATAA TGAAACGAAA TATCAGTAAT AGACAGGAAC TGGCAGATTC TTCTTCTAAT 3840 GAAGTAAGTA CTGCTAAATC TCCAAAATTA GATAAAAATG ATACAGCAAA TACAGCTTCA 3900 TTCAACGAAT TACCTTTTAA TTTTTTCAGA CACACCTTAT TACAAACTAA CTAAGTCAGA 3960 TGATGAGAAA GTAAATATAA ATTTAACTTA TGGGTATAAT ATAATAAAGA TTCATGATAT 4020 TAATAATTTA CTTAACGATG TTAATAGACT TATTCCATCA ACCCCTTCAA ACCTTTCTGG 4080 ATATTATAAA ATACCAGTTA ATGATATTAA AATAGATTGT TTAAGAGATG TAAATAATTA 4140 TTTGGAGGTA AAGGATATAA AATTAGTCTA TCTTTCACAT GGAAATGAAT TACCTAATAT 4200 TAATAATTAT GATAGGAATT TTTTAGGATT TACAGCTGTT ATATGTATCA ACAATACAGG 4260 CAGATCTATG GTTATGGTAA AACACTGTAA CGGGAAGCAG CATTCTATGG TAACTGGCCT 4320 ATGTTTAATA GCCAGATCAT TTTACTCTAT AAACATTTTA CCACAAATAA TAGGATCCTC 4380 TAGATATTTA ATATTATATC TAACAACAAC AAAAAAATTT AACGATGTAT GGCCAGAAGT 4440 ATTTTCTACT AATAAAGATA AAGATAGTCT ATCTTATCTA CAAGATATGA AAGAAGATAA 4500 TCATTTAGTA GTAGCTACTA ATATGGAAAG AAATGTATAC AAAAACGTGG AAGCTTTTAT 4560 ATTAAATAGC ATATTACTAG AAGATTTAAA ATCTAGACTT AGTATAACAA AACAGTTAAA 4620 TGCCAATATC GATTCTATAT TTCATCATAA CAGTAGTACA TTAATCAGTG ATATACTGAA 4680 ACGATCTACA GACTCAACTA TGCAAGGAAT AAGCAATATG CCAATTATGT CTAATATTTT 4740 AACTTTAGAA CTAAAACGTT CTACCAATAC TAAAAATAGG ATACGTGATA GGCTGTTAAA 4800 AGCTGCAATA AATAGTAAGG ATGTAGAAGA AATACTTTGT TCTATACCTT CGGAGGAAAG 4860 AACTTTAGAA CAACTTAAGT TTAATCAAAC TTGTATTTAT GAAGGTACC 4909 3567 base pairs nucleic acid single linear DNA (genomic) unknown 33 AAGACTAATT TGTAAACCAT CTTACTCAAA ATATGTAACA ATAGTACGAT GCAATGAGTA 60 AGACAATAGG AAATCTATCT TATATACACA TAATTATTCT ATCAATTTTA CCAATTAGTT 120 AGTGTAATGT TATAAAAACT AATTAATCAC TCGAGCCCCT AGCAATAAAA ACTATTCCTC 180 CGTGTTCTTA ATCTTCTCGA TCTTTTGGAG GATGTTCTGC ACGGCGTCCG ACGGCGTTTT 240 GGCGCCCCCC ATGCCGGCAG AACCCGGTTG CGGCCCCGTA CCGCTCTTCT GGGGCGACGA 300 TAGGTCGAAA GCCACCGTTT TCATGCCCGT CGTGCTCTTG ACGGGGGAAC CTACGGCGGC 360 GGTCCCCGTC GAGCGGCGTG ATTGCAAAGC CGCGCTCGCC CCCGGTTTCA GGATGGAGGG 420 GGAGGCCACA GGCGGCGCAT TCGATACGCT GCTTTTGGCC GTAGACGACG GTGGGTAAAC 480 GGTGGTTACC GCGGGATACG TCGGCGTGGT CGAGGCGGCC CGGCTGGTGC CGGACAGGCG 540 ACCCGGCGCG CTACCGCTCA CGGGTACCGA GGGCGGTCGA CCTACCACCG CCTTGCCGCC 600 CAAAGTAGGT TTCAAAGAAG GAACACCGAC GCGGCTGCCC CGACCTTTCA CCGGAGACGG 660 AGGGGCACTC TTGGCCGGGG ACGGAGAGGC TGACGAAAGC ATGGACAGCG GCGACGTGAC 720 GGGGGACACG ACATCATCCT CCGTGGGCGA CAAAACGGAC GCCGAGGCTG ACGGCTGTCG 780 AGCCGAAGCG GAAGAGGTTC TCGCGCCAGA AGTCACGTTC CTTGATGACG TTGTTTTAGA 840 CGAAGCCGGT TGAGGTTGCA ACAGCGTGGC GGGTACCGTC GACGGCGTGC CCGATACCTG 900 TTTCTCTACC CTTCCCTGAA CCGGTGTCGA CGTCACCGTC TGCGCTCGGG CGGACGCGTG 960 CGGCGTCGCG ACTCGCTTGC CCAGCACCGG TTTCTGGCTC GTGGATGTCG TCGTCATTGG 1020 AGACGATAAC TTAGCTTTAC GTATTCTGGA CGGCGTCGAC TGCTCGGGCG TCTGACTGGG 1080 AGGCGAAATG ACGTCGTTGT AATCGGACGA CGGTGTTGTG TGTCCCAGGC TGACGACGGA 1140 GCCGGTGTCC GAGGAGTCGT CGTCTTCCTC CTCGCTGTCT TCGACCGGTG ACTCTGCAGT 1200 TTGGTCCCTT AAAGCCCAAA CCTCATCAGC GGCGTTCTGA GACGCTGTTT GTGTCACCGC 1260 GGCGCGTGGA GTCGACGGCC TCCGAGGGGT GGTGGACACG TTGTTTTGAG AAGTCGTGGA 1320 AGTCGTAGGC ATCCTGAAGG GATTGTAAGC CAGGTGAGGA TTCTTGAGGG CCCACGCGCG 1380 TTCGCGCGGC CAGTTGGCGG GGTTCATATC CCCGGGCAAC GGCGCCGTCG GAGCCCAGGG 1440 CGAGTTACCG TTGACCGGGG TTTGGGTACC CGCGAAGGTA GGTGTCGGGG CCGGAGCGGG 1500 GGCCGTGGAA GGATTGACAG GCGTCGGCGT GAGGATGGCA GCGCCGGCGC CAGCAGGGAC 1560 GTTAACTCCG GCGCCGAACG TCAACGTCGG TTGCTCGAAC TTGTACGCGG TGGTGACGGG 1620 CGGTTTGGCG CTCGTCTCGG TATCCGTGAT GTCCACCAGC GTGTCGGTGA AACGCGGATC 1680 TTGACGGTTG GGGGGATAGC CATCCGAGCT GTCGGAATCC TCGTCGCCCG AGAAAAGATC 1740 CCCTCTTGTC TCCGTGAGCG GCCTCACGTC CCACGCGCTG TCCCGACGGA CCCTTCCCGG 1800 GCTGGCCTTG GTTACCTGCG GGGAGACGAG ACTGAAAGCC GCGTGACGCT GTTGTTGCTG 1860 CGGGATGTTC AAGGGACCGC TGGTCGGTTT CTGACTGCCC GAGGATAACA TGCCGCTGAA 1920 AATGCTGGAA ACACCGTTGC CACTAGCGGC GCCCTTGCCG CTAGTTCCCG GTTTCTTGAT 1980 GGGCGTAAAG ATGTTTTTCT CGTCATCATC ATCGTCGTCG TCCTCATCGG CACTGGAGCC 2040 AAAGAGCCTC CGGGAGGCGC CCGGTTTACG TGTCGGGGGC GGCGGTTGCT GCTGACGTTG 2100 CTGCAGGTTC TGCTGCCTCT CCTCCCAAGC CTTCAGCTGC TGTTTCTCAC GCTGCACCAC 2160 CTCGTCGTCC ACCCGTTTCT GCCGCTCGCG ACGCTTTTCC TCTTCGTCGT AATAGCCGAC 2220 GCGCGCCGAA CGGGCGGCGT GGGCGTCGGC GGCCGGTGCC AGAGAACCAT GGGCCTCGAA 2280 GCGGAACGGT TTGTGTCCCT TCCAGGGACT GGCGATCCAG CTCCAGCCGT CCAGCGGCTG 2340 CGTGGGGACA TGTTTCTTGG GTACCGACGA GAAGGCTGAA CCGCCGCCGA GCGAGAGGAG 2400 ATTGGCGTCA TCGTCAAACT CCAACGACGG CGGGCGCGCG CCCAAAAAGG TGTGCGCCGA 2460 CTGCGGGAAG CTGTCCACGT AGATGTCAAA GTCCTCGATG AGCAGCTCCA GCAGCGTGTC 2520 GGCCGAGTCA CCGTTTTCCA CGGCGTGTTT GAGGATATTG CGACAGTAGT TGGAATCAAA 2580 GGAAAGGCAC ATGCGCAGCT CCTTGACCAG CAGCTTGCAG CGCTCCTGAA TGCGCGCCAG 2640 ACATTTGCGC TCCAGCTCCT CCCAAGACCT GCGCACGTTC ATGATGAGAC GGCCCGTGTA 2700 CACGAGCTTG TTGACGGCGT TGACCAGCGC CGTGTTGGCG TGCCGGTCCA GGTTAAGGTC 2760 GAGCGGTTTC ACGCAGAACA TGTTACGGCG CACACCCTCC AGGTTTTCTT CAATGCGCTG 2820 CACCTCCGTA TCCTTGAGGT GCACAAAAGC GATGGGTTCC GTCTGGCCGA TGGCTGTGAC 2880 CAGCGTCTCG CGCACCGACA TCTTGGCCAG AATGACCGCG CTTACGAGCG CGCGCTCCAC 2940 AATCTCAGCA TCGTGGCGTA CGTCCGTATC GAATTCGGTA CGGTCTAGCA CAGCCAGGTG 3000 GTCACGCGCC TTACCACGAT CACCGAACGG GTAAGTGTAG CCGCGACGCG CCACGGCCGC 3060 GCAACGCACC TCGAACTCCT CGAGAACCGA GGAGAGGTCG GGGTTGTGGA AACGCAGCTC 3120 GCGGTAGTAT CCCAACCAAA GCATGAGCTC GTTGAACAGC ACCGTACGCC GGTGCAGGCG 3180 TTTTTCGCCA CATTTTTTCA GGATCTTGGG GTGTGCCTCG AGATCCACGT CGGGCTTTTG 3240 CGTGAGATGG CGCAGAAAGT TGACCAGGGC CACCACATCG CGCCGCTGTA GACCGATAAA 3300 CTGCAAACTC ATTTTATATT GTAATTATAT ATTTTCAATT TTGAAATCCC AAAATATTAT 3360 CATATCTTCC CAATAAAGCT AGGGGGAATT CGGATCCTCG CGACTGCAGG GTACCTGAGT 3420 AGCTAATTTT TAAACAAAAA TGTGGGAGAA TCTAATTAGT TTTTCTTTAC ACAATTGACG 3480 TACATGAGTC TGAGTTCCTT GTTTTTGCTA ATTATTTCAT CCAATTTATT ATTCTTGACG 3540 ATATCGAGAT CTTTTGTATA GGAGTCA 3567 4893 base pairs nucleic acid single linear DNA (genomic) unknown 34 CTGCAGGTCG ACGGATCTGA GAATGGATGA TTCTCCAGCC GAAACATATT CTACCATGGC 60 TCCGTTTAAT TTGTTGATGA AGATGGATTC ATCCTTAAAT GTTTTCTCTG TAATAGTTTC 120 CACCGAAAGA CTATGCAAAG AATTTGGAAT GCGTTCCTTG TGCTTAATGT TTCCATAGAC 180 GGCTTCTAGA AGTTGATACA ACATAGGACT AGCCGCGGTA ACTTTTATTT TTAGAAAGTA 240 TCCATCGCTT CTATCTTGTT TAGATTTATT TTTATAAAGT TTAGTCTCTC CTTCCAACAT 300 AATAAAAGTG GAAGTCATTT GACTAGATAA ACTATCAGTA AGTTTTATAG AGATAGACGA 360 ACAATTAGCG TATTGAGAAG CATTTAGTGT AACGTATTCG ATACATTTTG CATTAGATTT 420 ACTAATCGAT TTTGCATACT CTATAACACC CGCACAAGTC TGTAGAGAAT CGCTAGATGC 480 AGTAGGTCTT GGTGAAGTTT CAACTCTCTT CTTGATTACC TTACTCATGA TTAAACCTAA 540 ATAATTGTAC TTTGTAATAT AATGATATAT ATTTTCACTT TATCTCATTT GAGAATAAAA 600 AGATCACAAA AATTAACTAA TCAGGATCTC GAGATAAAAA TCAGCATGTC TTGAGCATGC 660 GGTAGAGCAG ATAGATGCCG ATGATGGCCG ATAGCGCGTA GACGGACATC ATGAGGAGAC 720 GACTGTCGGT AGCGTCCACG ACGACGTCAG TTACTTCTAG GACCGTACCG TTTTTCAAAA 780 GCATGAGGTA GTGAGTTCGC GGAGATGAGA CCACCACTTC GTTGTAGGGA TCCAGGGCGA 840 AAAGGACGTC GTCCGAGTCG TGCATGTACA TGATGTTGAT GACGCCTTGC GTGTCGTCGT 900 ATTCTAGTAG GGCGCTTTGG CAAAAGGCGC AGTTTTCTAG GGAAATGTTG AGCGCCGCTG 960 TGATGCTGTG TGTGGTATGC ATGTTGCGCG TCAGTTCGCA TTTAGTTTGA CTGTCCGTCT 1020 GGGTGATGAT GAGGCTCTGG CCTACGACGG TGGTGGAGAC AGGGTAGGAG ATACCTTTGA 1080 TCAGGTACTG GTTTGTTACG ACATAACTGA CGTGTTCGGA GACGGTCAGC GCGGAGAAGG 1140 ATTCGCCGAG CGGCAGACAA AACAGGTCGG GGAAGGTTTC TAGCGTGCTT GGTTGCATGG 1200 TAGATAGGAT GGAGAGGGCG GCGGGAACGG TAGTGGGGAC GGTGGCATCG GGGAAGAGAC 1260 GTGTGAGGCG TTCGAGCGAG TGATCGCGTC GCCCGCTACT GGAACAGGGT GTGTACAGGT 1320 CGCTGAGGTA TTCGTGGTGC GGATGAGCTA GCAACTGCGT AAAGTGTGAT AGCTCGGCTA 1380 ATGAACAGAG GCCCGTTTCT ACGATGAAGA TTTCGCGTCT CTCCGTCGTA TGTACTAGCA 1440 TGGAGTGGAC GAGGCTGCCC ATGAGGTAGA GTTCTTGACG CGCGAAGGCT GAAAGAAAAG 1500 AGGCCAGGTG CGTTTTGTGT AGTTTTAGGG CAAAGTCGGC GATCTGTCGT AGTGCCCACT 1560 GGGGGATGAG ATGTTGCTGA TTCTGTTTAG AGAGTATGTA GACCAGGCGT ACGAGGCTGG 1620 TGATGTCGGT GATCTGATTC GGTGTCCAAA GGGCTCGTTT GGCCAGGTCC ACGGCCGTGG 1680 GATACAGCAG CAACGTGGTG CGTGGTGGTG TTTGTGAGAG GCAGGTGATC ATAAATTCTT 1740 GTATTTGTAA GAGTGCGGCC TGGCGGTCTA GGGCCCGTGG GACGGAGACT TGGGCGCCGG 1800 CCTCTTCTTG TCGGGCTGCT GCGAACAGTG CTAATGCGTA GGCGAAGGCC ATTTCTACCG 1860 TGCGGCGGTC CAGCATCTGA CATCGACCGC TTTTGAGTAC ATCCACGGCG TAACGGTGAA 1920 AGCTGTTACG TAGTAGTGCG CTGAGGTCCA GGTAGTTGAA GTCAAGTGCG GCGTCAAGAA 1980 AGTCCGGGTC TTTGAGATAA GAGTGACGGT TCAGTTGATC TTTCTTAACT AGCACCAGGA 2040 GCTCGTGTTT TTCAGTTTGT CGTAGTATAA AGTTGTCGCG TTGATAGGGC GCTTTAAAGA 2100 GTACGCGTGG AAGATGGCCG AAGATAAGCA GCATGGGTGT GTCGTCGTCT ATGGACACCG 2160 TAACTACGAA GAAGTCCTCG GTCAGTGTTA TTTTAACGTA ACGTAGTTCG TCGATGAGGT 2220 AAAAGCCTTG GTGCAAACAA GGTGTGACGG TGCTGAATAG TAGATCGTGT CCATCAAAGA 2280 GGATACAGGT CTGGTTAAAG TGTGGTCGGT GTAGTCCTGA GGTGGTATGT GATTCTGTCC 2340 AGCCGTGTGG AGTGGTTTGC GGTGGCATCC AAACGTGAGG TATTGACAGG TCAATGGGTG 2400 GTGGCACAGT GGTGGGCTGT TCACCTAGGC TGTCCTGTGC CTTTAGCTGC TGCGAAAAAG 2460 ATCGGTAGCT GGCCAGGTCT TTGGATACCA GCGCGTAAGT GTTAAGTCTC TGTTGGTATC 2520 TTTCCAGGGT TTCGGTCAGA TCTACCTGGT TCAGAAACTG CTCCGCCAGA GGACCCGCAA 2580 AAAGACATCG AGGCATATGG AATACATAGT ATTGATTATA GCTTTGGAAA AAGTTGAAAC 2640 TGATGGCGTT TTCCCTGACG ACCGTGCTGT TACGGAGGCT GCTATTGTAG GTACACTGGG 2700 TGGTGTTTTC ACGCAGGAAG CGGATGGGTC TCCCGTAGGT GTTGAGCAGT AGGTGAAACG 2760 CTTTGTCCAG CGGTTCGGAT ATGGCTTCTG CGCCATATCG TGACGAAAGT AGGTGGCTGA 2820 GGAGACAGAC GGCGAGGACG ATGAGGTAGG AGGGGAGCCC GGGCCGCATT TTATATTGTA 2880 ATTATATATT TTCAATTTTG AAATCCCAAA ATATTATCAT ATTCTTCCCA ATAAACTCGA 2940 GATCCTTCTT TATTCTATAC TTAAAAAGTG AAAATAAATA CAAAGGTTCT TGAGGGTTGT 3000 GTTAAATTGA AAGCGAGAAA TAATCATAAA TTATTTCATT ATCGCGATAT CCGTTAAGTT 3060 TGTATCGTAA TGAAACAGAT TAAGGTTCGA GTGGACATGG TGCGGCATAG AATCAAGGAG 3120 CACATGCTGA AAAAATATAC CCAGACGGAA GAGAAATTCA CTGGCGCCTT TAATATGATG 3180 GGAGGATGTT TGCAGAATGC CTTAGATATC TTAGATAAGG TTCATGAGCC TTTCGAGGAG 3240 ATGAAGTGTA TTGGGCTAAC TATGCAGAGC ATGTATGAGA ACTACATTGT ACCTGAGGAT 3300 AAGCGGGAGA TGTGGATGGC TTGTATTAAG GAGCTGCATG ATGTGAGCAA GGGCGCCGCT 3360 AACAAGTTGG GGGGTGCACT GCAGGCTAAG GCCCGTGCTA AAAAGGATGA ACTTAGGAGA 3420 AAGATGATGT ATATGTGCTA CAGGAATATA GAGTTCTTTA CCAAGAACTC AGCCTTCCCT 3480 AAGACCACCA ATGGCTGCAG TCAGGCCATG GCGGCACTGC AGAACTTGCC TCAGTGCTCC 3540 CCTGATGAGA TTATGGCTTA TGCCCAGAAA ATATTTAAGA TTTTGGATGA GGAGAGAGAC 3600 AAGGTGCTCA CGCACATTGA TCACATATTT ATGGATATCC TCACTACATG TGTGGAAACA 3660 ATGTGTAATG AGTACAAGGT CACTAGTGAC GCTTGTATGA TGACCATGTA CGGGGGCATC 3720 TCTCTCTTAA GTGAGTTCTG TCGGGTGCTG TGCTGCTATG TCTTAGAGGA GACTAGTGTG 3780 ATGCTGGCCA AGCGGCCTCT GATAACCAAG CCTGAGGTTA TCAGTGTAAT GAAGCGCCGC 3840 ATTGAGGAGA TCTGCATGAA GGTCTTTGCC CAGTACATTC TGGGGGCCGA TCCTCTGAGA 3900 GTCTGCTCTC CTAGTGTGGA TGACCTACGG GCCATCGCCG AGGAGTCAGA TGAGGAAGAG 3960 GCTATTGTAG CCTACACTTT GGCCACCGCT GGTGTCAGCT CCTCTGATTC TCTGGTGTCA 4020 CCCCCAGAGT CCCCTGTACC CGCGACTATC CCTCTGTCCT CAGTAATTGT GGCTGAGAAC 4080 AGTGATCAGG AAGAAAGTGA GCAGAGTGAT GAGGAAGAGG AGGAGGGTGC TCAGGAGGAG 4140 CGGGAGGACA CTGTGTCTGT CAAGTCTGAG CCAGTGTCTG AGATAGAGGA AGTTGCCCCA 4200 GAGGAAGAGG AGGATGGTGC TGAGGAACCC ACCGCCTCTG GAGGTAAGAG TACCCACCCT 4260 ATGGTGACTA GAAGCAAGGC TGACCAGTAA TTTTTATCTC GAGCCCGGGA GATCTTAGCT 4320 AACTGATTTT TCTGGGAAAA AAATTATTTA ACTTTTCATT AATAGGGATT TGACGTATGT 4380 AGCGTACAAA ATTATCGTTC CTGGTATATA GATAAAGAGT CCTATATATT TGAAAATCGT 4440 TACGGCTCGA TTAAACTTTA ATGATTGCAT AGTGAATATA TCATTAGGAT TTAACTCCTT 4500 GACTATCATG GCGGCGCCAG AAATTACCAT CAAAAGCATT AATACAGTTA TGCCGATCGC 4560 AGTTAGAACG GTTATAGCAT CCACCATTTA TATCTAAAAA TTAGATCAAA GAATATGTGA 4620 CAAAGTCCTA GTTGTATACT GAGAATTGAC GAAACAATGT TTCTTACATA TTTTTTTCTT 4680 ATTAGTAACT GACTTAATAG TAGGAACTGG AAAGCTAGAC TTGATTATTC TATAAGTATA 4740 GATACCCTTC CAGATAATGT TCTCTTTGAT AAAAGTTCCA GAAAATGTAG AATTTTTTAA 4800 AAAGTTATCT TTTGCTATTA CCAAGATTGT GTTTAGACGC TTATTATTAA TATGAGTAAT 4860 GAAATCCACA CCGCCTCTAG ATATGGGGAA TTC 4893 6749 base pairs nucleic acid single linear DNA (genomic) unknown 35 GAGCTCGCGG CCGCCTATCA AAAGTCTTAA TGAGTTAGGT GTAGATAGTA TAGATATTAC 60 TACAAAGGTA TTCATATTTC CTATCAATTC TAAAGTAGAT GATATTAATA ACTCAAAGAT 120 GATGATAGTA GATAATAGAT ACGCTCATAT AATGACTGCA AATTTGGACG GTTCACATTT 180 TAATCATCAC GCGTTCATAA GTTTCAACTG CATAGATCAA AATCTCACTA AAAAGATAGC 240 CGATGTATTT GAGAGAGATT GGACATCTAA CTACGCTAAA GAAATTACAG TTATAAATAA 300 TACATAATGG ATTTTGTTAT CATCAGTTAT ATTTAACATA AGTACAATAA AAAGTATTAA 360 ATAAAAATAC TTACTTACGA AAAAATGACT AATTAGCTAT AAAAACCCAA CAAAAACTAA 420 TCAGCTATCG GGGTTAATTA ATTAGTTATT AGACAAGGTG AAAACGAAAC TATTTGTAGC 480 TTAATTAATT AGAGCTTCTT TATTCTATAC TTAAAAAGTG AAAATAAATA CAAAGGTTCT 540 TGAGGGTTGT GTTAAATTGA AAGCGAGAAA TAATCATAAA TTATTTCATT ATGGCGATAT 600 CCGTTAAGTT TGTATCGTAA TGGAGTCGCG CGGTCGCCGT TGTCCCGAAA TGATATCCGT 660 ACTGGGTCCC ATTTCGGGGC ACGTGCTGAA AGCCGTGTTT AGTCGCGGCG ACACGCCGGT 720 GCTGCCGCAC GAGACGCGAC TCCTGCAGAC GGGTATCCAC GTGCGCGTGA GCCAGCCCTC 780 GCTGATCCTG GTGTCGCAGT ACACGCCCGA CTCGACGCCA TGCCACCGCG GCGACAATCA 840 GCTGCAGGTG CAGCACACGT ACTTTACGGG CAGCGAGGTG GAGAACGTGT CGGTCAACGT 900 GCACAACCCC ACGGGCCGGA GCATCTGCCC CAGCCAAGAG CCCATGTCGA TCTATGTGTA 960 CGCGCTGCCG CTCAAGATGC TGAACATCCC CAGCATCAAC GTGCACCACT ACCCGTCGGC 1020 GGCCGAGCGC AAACACCGAC ACCTGCCCGT AGCTGACGCT GTGATTCACG CGTCGGGCAA 1080 GCAGATGTGG CAGGCGCGTC TCACGGTCTC GGGACTGGCC TGGACGCGTC AGCAGAACCA 1140 GTGGAAAGAG CCCGACGTCT ACTACACGTC AGCGTTCGTG TTTCCCACCA AGGACGTGGC 1200 ACTGCGGCAC GTGGTGTGCG CGCACGAGCT GGTTTGCTCC ATGGAGAACA CGCGCGCAAC 1260 CAAGATGCAG GTGATAGGTG ACCAGTACGT CAAGGTGTAC CTGGAGTCCT TCTGCGAGGA 1320 CGTGCCCTCC GGCAAGCTCT TTATGCACGT CACGCTGGGC TCTGACGTGG AAGAGGACCT 1380 GACGATGACC CGCAACCCGC AACCCTTCAT GCGCCCCCAC GAGCGCAACG GCTTTACGGT 1440 GTTGTGTCCC AAAAATATGA TAATCAAACC GGGCAAGATC TCGCACATCA TGCTGGATGT 1500 GGCTTTTACC TCACACGAGC ATTTTGGGCT GCTGTGTCCC AAGAGCATCC CGGGCCTGAG 1560 CATCTCAGGT AACCTATTGA TGAACGGGCA GCAGATCTTC CTGGAGGTGC AAGCGATACG 1620 CGAGACCGTG GAACTGCGTC AGTACGATCC CGTGGCTGCG CTCTTCTTTT TCGATATCGA 1680 CTTGCTGCTG CAGCGCGGGC CTCAGTACAG CGAACACCCC ACCTTCACCA GCCAGTATCG 1740 CATCCAGGGC AAGCTTGAGT ACCGACACAC CTGGGACCGG CACGACGAGG GTGCCGCCCA 1800 GGGCGACGAC GACGTCTGGA CCAGCGGATC GGACTCCGAC GAGGAACTCG TAACCACCGA 1860 GCGCAAGACG CCCCGCGTTA CCGGCGGCGG CGCCATGGCG GGCGCCTCCA CTTCCGCGGG 1920 CCGCAAACGC AAATCAGCAT CCTCGGCGAC GGCGTGCACG GCGGGCGTTA TGACACGCGG 1980 CCGCCTTAAG GCCGAGTCCA CCGTCGCGCC CGAAGAGGAC ACCGACGAGG ATTCCGACAA 2040 CGAAATCCAC AATCCGGCCG TGTTCACCTG GCCGCCCTGG CAGGCCGGCA TCCTGGCCCG 2100 CAACCTGGTG CCCATGGTGG CTACGGTTCA GGGTCAGAAT CTGAAGTACC AGGAGTTCTT 2160 CTGGGACGCC AACGACATCT ACCGCATCTT CGCCGAATTG GAAGGCGTAT GGCAGCCCGC 2220 TGCGCAACCC AAACGTCGCC GCCACCGGCA AGACGCCTTG CCCGGGCCAT GCATCGCCTC 2280 GACGCCCAAA AAGCACCGAG GTTGATTTTT ATGGATCCGG TACCCTCGAG GAATTCTAGC 2340 AATAAAAACT ATTCCTCCGT GTTCTTAATC TTCTCGATCT TTTGGAGGAT GTTCTGCACG 2400 GCGTCCGACG GCGTTTTGGC GCCCCCCATG CCGGCAGAAC CCGGTTGCGG CCCCGTACCG 2460 CTCTTCTGGG GCGACGATAG GTCGAAAGCC ACCGTTTTCA TGCCCGTCGT GCTCTTGACG 2520 GGGGAACCTA CGGCGGCGGT CCCCGTCGAG CGGCGTGATT GCAAAGCCGC GCTCGCCCCC 2580 GGTTTCAGGA TGGAGGGGGA GGCCACAGGC GGCGCATTCG ATACGCTGCT TTTGGCCGTA 2640 GACGACGGTG GGTAAACGGT GGTTACCGCG GGATACGTCG GCGTGGTCGA GGCGGCCCGG 2700 CTGGTGCCGG ACAGGCGACC CGGCGCGCTA CCGCTCACGG GTACCGAGGG CGGTCGACCT 2760 ACCACCGCCT TGCCGCCCAA AGTAGGTTTC AAAGAAGGAA CACCGACGCG GCTGCCCCGA 2820 CCTTTCACCG GAGACGGAGG GGCACTCTTG GCCGGGGACG GAGAGGCTGA CGAAAGCATG 2880 GACAGCGGCG ACGTGACGGG GGACACGACA TCATCCTCCG TGGGCGACAA AACGGACGCC 2940 GAGGCTGACG GCTGTCGAGC CGAAGCGGAA GAGGTTCTCG CGCCAGAAGT CACGTTCCTT 3000 GATGACGTTG TTTTAGACGA AGCCGGTTGA GGTTGCAACA GCGTGGCGGG TACCGTCGAC 3060 GGCGTGCCCG ATACCTGTTT CTCTACCCTT CCCTGAACCG GTGTCGACGT CACCGTCTGC 3120 GCTCGGGCGG ACGCGTGCGG CGTCGCGACT CGCTTGCCCA GCACCGGTTT CTGGCTCGTG 3180 GATGTCGTCG TCATTGGAGA CGATAACTTA GCTTTACGTA TTCTGGACGG CGTCGACTGC 3240 TCGGGCGTCT GACTGGGAGG CGAAATGACG TCGTTGTAAT CGGACGACGG TGTTGTGTGT 3300 CCCAGGCTGA CGACGGAGCC GGTGTCCGAG GAGTCGTCGT CTTCCTCCTC GCTGTCTTCG 3360 ACCGGTGACT CTGCAGTTTG GTCCCTTAAA GCCCAAACCT CATCAGCGGC GTTCTGAGAC 3420 GCTGTTTGTG TCACCGCGGC GCGTGGAGTC GACGGCCTCC GAGGGGTGGT GGACACGTTG 3480 TTTTGAGAAG TCGTGGAAGT CGTAGGCATC CTGAAGGGAT TGTAAGCCAG GTGAGGATTC 3540 TTGAGGGCCC ACGCGCGTTC GCGCGGCCAG TTGGCGGGGT TCATATCCCC GGGCAACGGC 3600 GCCGTCGGAG CCCAGGGCGA GTTACCGTTG ACCGGGGTTT GGGTACCCGC GAAGGTAGGT 3660 GTCGGGGCCG GAGCGGGGGC CGTGGAAGGA TTGACAGGCG TCGGCGTGAG GATGGCAGCG 3720 CCGGCGCCAG CAGGGACGTT AACTCCGGCG CCGAACGTCA ACGTCGGTTG CTCGAACTTG 3780 TACGCGGTGG TGACGGGCGG TTTGGCGCTC GTCTCGGTAT CCGTGATGTC CACCAGCGTG 3840 TCGGTGAAAC GCGGATCTTG ACGGTTGGGG GGATAGCCAT CCGAGCTGTC GGAATCCTCG 3900 TCGCCCGAGA AAAGATCCCC TCTTGTCTCC GTGAGCGGCC TCACGTCCCA CGCGCTGTCC 3960 CGACGGACCC TTCCCGGGCT GGCCTTGGTT ACCTGCGGGG AGACGAGACT GAAAGCCGCG 4020 TGACGCTGTT GTTGCTGCGG GATGTTCAAG GGACCGCTGG TCGGTTTCTG ACTGCCCGAG 4080 GATAACATGC CGCTGAAAAT GCTGGAAACA CCGTTGCCAC TAGCGGCGCC CTTGCCGCTA 4140 GTTCCCGGTT TCTTGATGGG CGTAAAGATG TTTTTCTCGT CATCATCATC GTCGTCGTCC 4200 TCATCGGCAC TGGAGCCAAA GAGCCTCCGG GAGGCGCCCG GTTTACGTGT CGGGGGCGGC 4260 GGTTGCTGCT GACGTTGCTG CAGGTTCTGC TGCCTCTCCT CCCAAGCCTT CAGCTGCTGT 4320 TTCTCACGCT GCACCACCTC GTCGTCCACC CGTTTCTGCC GCTCGCGACG CTTTTCCTCT 4380 TCGTCGTAAT AGCCGACGCG CGCCGAACGG GCGGCGTGGG CGTCGGCGGC CGGTGCCAGA 4440 GAACCATGGG CCTCGAAGCG GAACGGTTTG TGTCCCTTCC AGGGACTGGC GATCCAGCTC 4500 CAGCCGTCCA GCGGCTGCGT GGGGACATGT TTCTTGGGTA CCGACGAGAA GGCTGAACCG 4560 CCGCCGAGCG AGAGGAGATT GGCGTCATCG TCAAACTCCA ACGACGGCGG GCGCGCGCCC 4620 AAAAAGGTGT GCGCCGACTG CGGGAAGCTG TCCACGTAGA TGTCAAAGTC CTCGATGAGC 4680 AGCTCCAGCA GCGTGTCGGC CGAGTCACCG TTTTCCACGG CGTGTTTGAG GATATTGCGA 4740 CAGTAGTTGG AATCAAAGGA AAGGCACATG CGCAGCTCCT TGACCAGCAG CTTGCAGCGC 4800 TCCTGAATGC GCGCCAGACA TTTGCGCTCC AGCTCCTCCC AAGACCTGCG CACGTTCATG 4860 ATGAGACGGC CCGTGTACAC GAGCTTGTTG ACGGCGTTGA CCAGCGCCGT GTTGGCGTGC 4920 CGGTCCAGGT TAAGGTCGAG CGGTTTCACG CAGAACATGT TACGGCGCAC ACCCTCCAGG 4980 TTTTCTTCAA TGCGCTGCAC CTCCGTATCC TTGAGGTGCA CAAAAGCGAT GGGTTCCGTC 5040 TGGCCGATGG CTGTGACCAG CGTCTCGCGC ACCGACATCT TGGCCAGAAT GACCGCGCTT 5100 ACGAGCGCGC GCTCCACAAT CTCAGCATCG TGGCGTACGT CCGTATCGAA TTCGGTACGG 5160 TCTAGCACAG CCAGGTGGTC ACGCGCCTTA CCACGATCAC CGAACGGGTA AGTGTAGCCG 5220 CGACGCGCCA CGGCCGCGCA ACGCACCTCG AACTCCTCGA GAACCGAGGA GAGGTCGGGG 5280 TTGTGGAAAC GCAGCTCGCG GTAGTATCCC AACCAAAGCA TGAGCTCGTT GAACAGCACC 5340 GTACGCCGGT GCAGGCGTTT TTCGCCACAT TTTTTCAGGA TCTTGGGGTG TGCCTCGAGA 5400 TCCACGTCGG GCTTTTGCGT GAGATGGCGC AGAAAGTTGA CCAGGGCCAC CACATCGCGC 5460 CGCTGTAGAC CGATAAACTG CAAACTCATT TTATATTGTA ATTATATATT TTCAATTTTG 5520 AAATCCCAAA ATATTATCAT ATCTTCCCAA TAAAGCTAGA ATTCTTTTTA TTGATTAACT 5580 AGTCAAATGA GTATATATAA TTGAAAAAGT AAAATATAAA TCATATAATA ATGAAACGAA 5640 ATATCAGTAA TAGACAGGAA CTGGCAGATT CTTCTTCTAA TGAAGTAAGT ACTGCTAAAT 5700 CTCCAAAATT AGATAAAAAT GATACAGCAA ATACAGCTTC ATTCAACGAA TTACCTTTTA 5760 ATTTTTTCAG ACACACCTTA TTACAAACTA ACTAAGTCAG ATGATGAGAA AGTAAATATA 5820 AATTTAACTT ATGGGTATAA TATAATAAAG ATTCATGATA TTAATAATTT ACTTAACGAT 5880 GTTAATAGAC TTATTCCATC AACCCCTTCA AACCTTTCTG GATATTATAA AATACCAGTT 5940 AATGATATTA AAATAGATTG TTTAAGAGAT GTAAATAATT ATTTGGAGGT AAAGGATATA 6000 AAATTAGTCT ATCTTTCACA TGGAAATGAA TTACCTAATA TTAATAATTA TGATAGGAAT 6060 TTTTTAGGAT TTACAGCTGT TATATGTATC AACAATACAG GCAGATCTAT GGTTATGGTA 6120 AAACACTGTA ACGGGAAGCA GCATTCTATG GTAACTGGCC TATGTTTAAT AGCCAGATCA 6180 TTTTACTCTA TAAACATTTT ACCACAAATA ATAGGATCCT CTAGATATTT AATATTATAT 6240 CTAACAACAA CAAAAAAATT TAACGATGTA TGGCCAGAAG TATTTTCTAC TAATAAAGAT 6300 AAAGATAGTC TATCTTATCT ACAAGATATG AAAGAAGATA ATCATTTAGT AGTAGCTACT 6360 AATATGGAAA GAAATGTATA CAAAAACGTG GAAGCTTTTA TATTAAATAG CATATTACTA 6420 GAAGATTTAA AATCTAGACT TAGTATAACA AAACAGTTAA ATGCCAATAT CGATTCTATA 6480 TTTCATCATA ACAGTAGTAC ATTAATCAGT GATATACTGA AACGATCTAC AGACTCAACT 6540 ATGCAAGGAA TAAGCAATAT GCCAATTATG TCTAATATTT TAACTTTAGA ACTAAAACGT 6600 TCTACCAATA CTAAAAATAG GATACGTGAT AGGCTGTTAA AAGCTGCAAT AAATAGTAAG 6660 GATGTAGAAG AAATACTTTG TTCTATACCT TCGGAGGAAA GAACTTTAGA ACAACTTAAG 6720 TTTAATCAAA CTTGTATTTA TGAAGGTAC 6749 837 base pairs nucleic acid single linear DNA (genomic) unknown 36 ATGTGCCGCC GCCCGGATTG CGGCTTCTCT TTCTCACCTG GACCGGTGGC ACTGCTGTGG 60 TGTTGCCTTC TGCTGCCCAT CGTTTCCTCA GCCACCGTCA GCGTCGCTCC TACCGTCGCC 120 GAGAAAGTTC CCGCGGAGTG CCCCGAACTA ACGCGTCGAT GCCTGTTGGG TGAGGTGTTT 180 CAGGGTGACA AGTATGAAAG TTGGCTGCGC CCGTTGGTGA ATGTTACCAG ACGCGATGGC 240 CCGCTATCGC AACTTATTCG TTACCGTCCC GTTACGCCGG AGGCCGCCAA CTCCGTGCTG 300 TTGGACGATG CTTTCCTGGA CACTCTGGCC CTGCTGTACA ACAATCCGGA TCAATTGCGG 360 GCCTTGCTGA CGCTGTTGAG CTCGGACACA GCGCCGCGCT GGATGACGGT GATGCGCGGT 420 TACAGCGAGT GCGGCGATGG CTCGCCGGCC GTGTACACGT GCGTGGACGA CCTGTGCCGC 480 GGCTACGACC TCACGCGACT GTCATACGGG CGCAGCATCT TCACGGAACA CGTGTTAGGC 540 TTCGAGCTGG TGCCACCGTC TCTCTTTAAC GTGGTGGTGG CCATACGCAA CGAAGCCACG 600 CGTACCAACC GCGCCGTGCG TCTGCCCGTG AGCACCGCTG CCGCGCCCGA GGGCATCACG 660 CTCTTTTACG GCCTGTACAA CGCAGTGAAG GAATTCTGCC TGCGTCACCA GCTGGACCCG 720 CCGCTGCTAC GCCACCTAGA TAAATACTAC GCCGGACTGC CGCCCGAGCT GAAGCAGACG 780 CGCGTCAACC TGCCGGCTCA CTCGCGCTAT GGCCCTCAAG CAGTGGATGC TCGCTAA 837 5234 base pairs nucleic acid single linear DNA (genomic) unknown 37 AAGCTTTTGC GATCAATAAA TGGATCACAA CCAGTATCTC TTAACGATGT TCTTCGCAGA 60 TGATGATTCA TTTTTTAAGT ATTTGGCTAG TCAAGATGAT GAATCTTCAT TATCTGATAT 120 ATTGCAAATC ACTCAATATC TAGACTTTCT GTTATTATTA TTGATCCAAT CAAAAAATAA 180 ATTAGAAGCC GTGGGTCATT GTTATGAATC TCTTTCAGAG GAATACAGAC AATTGACAAA 240 ATTCACAGAC TCTCAAGATT TTAAAAAACT GTTTAACAAG GTCCCTATTG TTACAGATGG 300 AAGGGTCAAA CTTAATAAAG GATATTTGTT CGACTTTGTG ATTAGTTTGA TGCGATTCAA 360 AAAAGAATCC TCTCTAGCTA CCACCGCAAT AGATCCTATT AGATACATAG ATCCTCGTCG 420 CGATATCGCA TTTTCTAACG TGATGGATAT ATTAAAGTCG AATAAAGTGA ACAATAATTA 480 ATTCTTTATT GTCATCATGT AATTAACTAG CTACCCGGGA GATCTCTCGA GCTGCAGAAG 540 CTTATAAAAA TCACAAGTCT CTGTCACTTT TTTTGTCTAG TTTTTTTTTC TCCTCTTGGT 600 TCAGACGTTC TCTTCTTCGT CGGAGTCTTT CAAGTGTCGG TAGCCGTTTT TGCGGTGTCG 660 CAGTCGGTCT AGCAGGTTGG GCTTCTGTCC CTTGTCCTGC GTGCCAGTCT GTCCGTCCAA 720 AGAATCTGTA CCGTTCTCGT GCGCTCGCTG CTCTGCGTCC AGACGGACCA GGGCCAGAAG 780 CATCTGGTAA GCCTGCTCGT TGGTGTAAGG CGGAGCCGCC GTGGATGCAT CAGACGACGG 840 TGGTCCCGGT CCTTTGCGAC CAGAATTATA AACACTTTCC TCGTAGGAAG GCGGAGCCTG 900 TAACGACGTG TCTTTGGTGT TGCCCGACGT CACGGTGGTC CCGTCGGCGG ACACCAGATA 960 GGGAAAGAGG TTCTGCAGCG GCTGCATGCA GAGACGCCGC TGTCGAGTAT AGATCAAATA 1020 AATGATAATG ACGACGGCTA TGGCCACGAG GATGATGGTG AAGGCTCCGA AGGGGTTTTT 1080 GAGGAAGGTG GCAACGCCTT CGACCACGGA GGCCACCGCG CCACCCACGG CCCCAATGGC 1140 TACGCCAACG GCCTTTCCCG CGGCGCCCAG GCCGCTCATG AGGTCGTCCA GACCCTTGAG 1200 GTAGGGCGGC AGCGGGTCGA CTACCTTGTC CTCCACGTAC TTTACCCGCT GCTTATACGA 1260 ATTGAACTCG CGCATGATCT CCTCGAGATC AAAAACGTTG CTGGAACGCA ATTCTTTCTG 1320 CGAGTAAAGT TCCAGTACCC TGAAGTCGGT GTTTTCCAGC GGGTCGATGT CTAGGGCGAT 1380 CATGCTGTCG ACGGTGGAGA TGCTGCTGAG GTCAATCATG CGTTTGAAGA GGTAGTCCAC 1440 GTACTCGTAG GCCGAGTTGC CGGCGATGAA GATCTTGAGG CTGGGAAGCT GACATTCCTC 1500 AGTGCGGTGG TTGCCCAACA GGATTTCGTT ATCCTCGCCC AGTTGACCGT ACTGCACGTA 1560 CGAGCTGTTG GCGAAATTAA AGATGACCAC TGGTCGTGAG TAGCAGCGTC CTGGCGATTC 1620 CTTCACATTC ATATCACGCA GCACCTTGAC GCTGGTTTGG TTAATGGTCA CGCAGCTGGC 1680 CAGACCCAGG ACATCACCCA TGAAACGCGC GGCAATCGGT TTGTTGTAGA TGGCCGAGAG 1740 AATAGCTGAC GGGTTGATCT TGCTAAGTTC CTTGAAGACC TCTAGGGTGC GCCGTTGATC 1800 CACACACCAG GCTTCTGCGA TTTCGGCCAG CGCCCGGTTG ATGTAACCGC GCAACGTGTC 1860 ATAGGTGAAC TGCAGCTGGG CGTAGACCAG ATTGTGCACC GACTCCATGT TGGATAAATG 1920 AGTTGCATTG TTGCCATCTG TACTTCTTTT GGTTCTATTA TGAGTAAGAT TCAGACTGGA 1980 GCGGTTGGCC AAACGTTCGA GTTCCACCAG AGATTTTTGC TTGATACCTT GCCAGAACAC 2040 CACCAAACCA CCAGTGGTTT CAAAGACGGA CACGTTTCCA TATTTTTCAT ATGTTTGATT 2100 GTATGAAGTA TTGAAAATCT GCTGTAACTT ATTTATGGCC TCATCACGTA CACAGTCCAG 2160 CCCAGAGTCG GACATGTTCA CCTCTTGCTT CTTAGATAAG AAAGTGGCGG TCATTTTGGC 2220 AGAAGAAAAG TGATACGAGT CCTCGGCTTC GGAACGAATG GTGCGTTCCG AGGCTTCCCA 2280 GAAAGTGAGT TGACAAGTAA CATTCTTCTC GTCCTGTATA TCCCAGGAGA TCACTGAGTC 2340 CGCACGTTCA AGAAAAGCCA CCAACCTGTG GGTCTCTAAC GCAGAATTCG GTCTTTCAAA 2400 GTCGGAGACG ATAGTGTAGT TCGGAAAAAT GAAAAACTTG TCGGCGTTTT CTCCAAAATA 2460 GCTGGCATTG CGATTAGTTC CGTTGTAGAA AGGAGAAATG TCAACCACAT CACCCGTGGA 2520 AGTTGCGAAA AAATGATAGG GATACTTGGA GCGCGCAGTA GTGATGGTCA CCATACAATT 2580 CAGATTACAG GTCTCACGAT AGAGCCAGGT GCTGCCGCGG CTGTGCCATT GATCCTTGAC 2640 CGTCACGTAA CGGGTACTGT GGGTGTTGGA ATAATCGTCG GGCATTAATT GCATGGTTTT 2700 GTTTTCATAG CTGTCCCTAT GATAAGCCAC GAAAACCGTG CCTGCTATAA CGCGGCTGTA 2760 GGAACTGTAG CACTGACTGT GACTGTTGAT ATGATGAATC TCCCACATAG GAGGCGCCAC 2820 GTATTCCGTG TTGCTGCCCA GCAGATAAGT GGTGTGGATG TAAGCGTAGC TACGACGAAA 2880 CGTCAAAACC TTCTGGTAGA CTCGTACCTT AAAGGTGTGC GCGACGATGT TGCGTTTGTA 2940 GACCACCATG ATGCCCTCGT CCAGGTCTTC ATTGATGGGC TTCATCGAGG TGCAGACGAT 3000 ATTACGTTCA AAGCGAATAA GATCCGTACC CTGTGCCATA GAACACACGC GATAGGGGTA 3060 CTTGGTGGTG TTGACCCCCA CCACATCTCC GTACTTGAGG GTAGTGTTGT AGATGGTCTC 3120 GTTAACACCA TGGCTGACCG TTTGGGAAGA AGTTACGCGT TGAGAGACTG AACCGGATCG 3180 AGAATGAGCA GCAGACGTCG TATGAGAGGA ATGGTGACTG TGAGTAGCAG AAGTTCCACG 3240 AGTAGAAGAT GAGGAAACCG CAGCACCCAG ACAGACGATA CACAAGTTAA CGCAGACTAC 3300 CAGGCACCAG ATCCTGGATT CCATTACGAT ACAAACTTAA CGGATATCGC GATAATGAAA 3360 TAATTTATGA TTATTTCTCG CTTTCAATTT AACACAACCC TCAAGAACCT TTGTATTTAT 3420 TTTCACTTTT AAGTATAGAA TAAAGAAGCT TGCATGCCAC GCGTCTCGAG GGCCCCTGCA 3480 GGTCGACTCT AGAGGATCCT TCTTTATTCT ATACTTAAAA AGTGAAAATA AATACAAAGG 3540 TTCTTGAGGG TTGTGTTAAA TTGAAAGCGA GAAATAATCA TAAATTATTT CATTATCGCG 3600 ATATCCGTTA AGTTTGTATC GTAATGTGCC GCCGCCCGGA TTGCGGCTTC TCTTTCTCAC 3660 CTGGACCGGT GGCACTGCTG TGGTGTTGCC TTCTGCTGCC CATCGTTTCC TCAGCCACCG 3720 TCAGCGTCGC TCCTACCGTC GCCGAGAAAG TTCCCGCGGA GTGCCCCGAA CTAACGCGTC 3780 GATGCCTGTT GGGTGAGGTG TTTCAGGGTG ACAAGTATGA AAGTTGGCTG CGCCCGTTGG 3840 TGAATGTTAC CAGACGCGAT GGCCCGCTAT CGCAACTTAT TCGTTACCGT CCCGTTACGC 3900 CGGAGGCCGC CAACTCCGTG CTGTTGGACG ATGCTTTCCT GGACACTCTG GCCCTGCTGT 3960 ACAACAATCC GGATCAATTG CGGGCCTTGC TGACGCTGTT GAGCTCGGAC ACAGCGCCGC 4020 GCTGGATGAC GGTGATGCGC GGTTACAGCG AGTGCGGCGA TGGCTCGCCG GCCGTGTACA 4080 CGTGCGTGGA CGACCTGTGC CGCGGCTACG ACCTCACGCG ACTGTCATAC GGGCGCAGCA 4140 TCTTCACGGA ACACGTGTTA GGCTTCGAGC TGGTGCCACC GTCTCTCTTT AACGTGGTGG 4200 TGGCCATACG CAACGAAGCC ACGCGTACCA ACCGCGCCGT GCGTCTGCCC GTGAGCACCG 4260 CTGCCGCGCC CGAGGGCATC ACGCTCTTTT ACGGCCTGTA CAACGCAGTG AAGGAATTCT 4320 GCCTGCGTCA CCAGCTGGAC CCGCCGCTGC TACGCCACCT AGATAAATAC TACGCCGGAC 4380 TGCCGCCCGA GCTGAAGCAG ACGCGCGTCA ACCTGCCGGC TCACTCGCGC TATGGCCCTC 4440 AAGCAGTGGA TGCTCGCTAA TTTTTATAGA TCCTGATCCT TTTTCTGGGT AAGTAATACG 4500 TCAAGGAGAA AACGAAACGA TCTGTAGTTA GCGGCCGCCT AATTAACTAA TATTATATTT 4560 TTTATCTAAA AAACTAAAAA TAAACATTGA TTAAATTTTA ATATAATACT TAAAAATGGA 4620 TGTTGTGTCG TTAGATAAAC CGTTTATGTA TTTTGAGGAA ATTGATAATG AGTTAGATTA 4680 CGAACCAGAA AGTGCAAATG AGGTCGCAAA AAAACTGCCG TATCAAGGAC AGTTAAAACT 4740 ATTACTAGGA GAATTATTTT TTCTTAGTAA GTTACAGCGA CACGGTATAT TAGATGGTGC 4800 CACCGTAGTG TATATAGGAT CGGCTCCTGG TACACATATA CGTTATTTGA GAGATCATTT 4860 CTATAATTTA GGAATGATTA TCAAATGGAT GCTAATTGAC GGACGCCATC ATGATCCTAT 4920 TTTAAATGGA TTGCGTGATG TGACTCTAGT GACTCGGTTC GTTGATGAGG AATATCTACG 4980 ATCCATCAAA AAACAACTGC ATCCTTCTAA GATTATTTTA ATTTCTGATG TGAGATCCAA 5040 ACGAGGAGGA AATGAACCTA GTACGGCGGA TTTACTAAGT AATTACGCTC TACAAAATGT 5100 CATGATTAGT ATTTTAAACC CCGTGGCGTC TAGTCTTAAA TGGAGATGCC CGTTTCCAGA 5160 TCAATGGATC AAGGACTTTT ATATCCCACA CGGTAATAAA ATGTTACAAC CTTTTGCTCC 5220 TTCATATTCA GCTG 5234 6749 base pairs nucleic acid single linear DNA (genomic) unknown 38 GAGCTCGCGG CCGCCTATCA AAAGTCTTAA TGAGTTAGGT GTAGATAGTA TAGATATTAC 60 TACAAAGGTA TTCATATTTC CTATCAATTC TAAAGTAGAT GATATTAATA ACTCAAAGAT 120 GATGATAGTA GATAATAGAT ACGCTCATAT AATGACTGCA AATTTGGACG GTTCACATTT 180 TAATCATCAC GCGTTCATAA GTTTCAACTG CATAGATCAA AATCTCACTA AAAAGATAGC 240 CGATGTATTT GAGAGAGATT GGACATCTAA CTACGCTAAA GAAATTACAG TTATAAATAA 300 TACATAATGG ATTTTGTTAT CATCAGTTAT ATTTAACATA AGTACAATAA AAAGTATTAA 360 ATAAAAATAC TTACTTACGA AAAAATGACT AATTAGCTAT AAAAACCCAA CAAAAACTAA 420 TCAGCTATCG GGGTTAATTA ATTAGTTATT AGACAAGGTG AAAACGAAAC TATTTGTAGC 480 TTAATTAATT AGAGCTTCTT TATTCTATAC TTAAAAAGTG AAAATAAATA CAAAGGTTCT 540 TGAGGGTTGT GTTAAATTGA AAGCGAGAAA TAATCATAAA TTATTTCATT ATGGCGATAT 600 CCGTTAAGTT TGTATCGTAA TGGAGTCGCG CGGTCGCCGT TGTCCCGAAA TGATATCCGT 660 ACTGGGTCCC ATTTCGGGGC ACGTGCTGAA ACCCGTGTTT AGTCGCGGCG ACACGCCGGT 720 GCTGCCGCAC GAGACGCGAC TCCTGCAGAC GGGTATCCAC GTGCGCGTGA GCCAGCCCTC 780 GCTGATCCTG GTGTCGCAGT ACACGCCCGA CTCGACGCCA TGCCACCGCG GCGACAATCA 840 GCTGCAGGTG CAGCACACGT ACTTTACGGG CAGCGAGGTG GAGAACGTGT CGGTCAACGT 900 GCACAACCCC ACGGGCCGGA GCATCTGCCC CAGCCAAGAG CCCATGTCGA TCTATGTGTA 960 CGCGCTGCCG CTCAAGATGC TGAACATCCC CAGCATCAAC GTGCACCACT ACCCGTCGGC 1020 GGCCGAGCGC AAACACCGAC ACCTGCCCGT AGCTGACGCT GTGATTCACG CGTCGGGCAA 1080 GTAGATGTGG CAGGCGCGTC TCACGGTCTC GGGACTGGCC TGGACGCGTC ACCAGAACCA 1140 GTGGAAAGAG CCCGACGTCT ACTACACGTC AGCGTTCGTG TTTCCCACCA AGGACGTGGC 1200 ACTGCGGCAC GTGGTGTGCG CGCACGAGCT GGTTTGCTCC ATGGAGAACA CGCGCGCAAC 1260 CAAGATGCAG GTGATAGGTG ACCAGTACGT CAAGGTGTAC CTGGAGTCCT TCTGCGAGGA 1320 CGTGCCCTCC GGCAAGCTCT TTATGCACGT CACGCTGGGC TCTGACGTGG AAGAGGACCT 1380 GACGATGACC CGCAACCCGC AACCCTTCAT GCGCCCCCAC GAGCGCAACG GCTTTACGGT 1440 GTTGTGTCCC AAAAATATGA TAATCAAACC GGGCAAGATC TCGCACATCA TGCTGGATGT 1500 GGCTTTTACC TCACACGAGC ATTTTGGGCT GCTGTGTCCC AAGAGCATCC CGGGCCTGAG 1560 CATCTCAGGT AACCTATTGA TGAACGGGCA GCAGATCTTC CTGGAGGTGC AAGCGATACG 1620 CGAGACCGTG GAACTGCGTC AGTACGATCC CGTGGCTGCG CTCTTCTTTT TCGATATCGA 1680 CTTGCTGCTG CAGCGCGGGC CTCAGTACAG CGAACACCCC ACCTTCACCA GCCAGTATCG 1740 CATCCAGGGC AAGCTTGAGT ACCGACACAC CTGGGACCGG CACGACGAGG GTGCCGCCCA 1800 GGGCGACGAC GACGTCTGGA CCAGCGGATC GGACTCCGAC GAGGAACTCG TAACCACCGA 1860 GCGCAAGACG CCCCGCGTTA CCGGCGGCGG CGCCATGGCG GGCGCCTCCA CTTCCGCGGG 1920 CCGCAAACGC AAATCAGCAT CCTCGGCGAC GGCGTGCACG GCGGGCGTTA TGACACGCGG 1980 CCGCCTTAAG GCCGAGTCCA CCGTCGCGCC CGAAGAGGAC ACCGACGAGG ATTCCGACAA 2040 CGAAATCCAC AATCCGGCCG TGTTCACCTG GCCGCCCTGG CAGGCCGGCA TCCTGGCCCG 2100 CAACCTGGTG CCCATGGTGG CTACGGTTCA GGGTCAGAAT CTGAAGTACC AGGAGTTCTT 2160 CTGGGACGCC AACGACATCT ACCGCATCTT CGCCGAATTG GAAGGCGTAT GGCAGCCCGC 2220 TGCGCAACCC AAACGTCGCC GCCACCGGCA AGACGCCTTG CCCGGGCCAT GCATCGCCTC 2280 GACGCCCAAA AAGCACCGAG GTTGATTTTT ATGGATCCGG TACCCTCGAG GAATTCTAGC 2340 TTTATTGGGA AGATATGATA ATATTTTGGG ATTTCAAAAT TGAAAATATA TAATTACAAT 2400 ATAAAATGAG TTTGCAGTTT ATCGGTCTAC AGCGGCGCGA TGTGGTGGCC CTGGTCAACT 2460 TTCTGCGCCA TCTCACGCAA AAGCCCGACG TGGATCTCGA GGCACACCCC AAGATCCTGA 2520 AAAAATGTGG CGAAAAACGC CTGCACCGGC GTACGGTGCT GTTCAACGAG CTCATGCTTT 2580 GGTTGGGATA CTACCGCGAG CTGCGTTTCC ACAACCCCGA CCTCTCCTCG GTTCTCGAGG 2640 AGTTCGAGGT GCGTTGCGCG GCCGTGGCGC GTCGCGGCTA CACTTACCCG TTCGGTGATC 2700 GTGGTAAGGC GCGTGACCAC CTGGCTGTGC TAGACCGTAC CGAATTCGAT ACGGACGTAC 2760 GCCACGATGC TGAGATTGTG GAGCGCGCGC TCGTAAGCGC GGTCATTCTG GCCAAGATGT 2820 CGGTGCGCGA GACGCTGGTC ACAGCCATCG GCCAGACGGA ACCCATCGCT TTTGTGCACC 2880 TCAAGGATAC GGAGGTGCAG CGCATTGAAG AAAACCTGGA GGGTGTGCGC CGTAACATGT 2940 TCTGCGTGAA ACCGCTCGAC CTTAACCTGG ACCGGCACGC CAACACGGCG CTGGTCAACG 3000 CCGTCAACAA GCTCGTGTAC ACGGGCCGTC TCATCATGAA CGTGCGCAGG TCTTGGGAGG 3060 AGCTGGAGCG CAAATGTCTG GCGCGCATTC AGGAGCGCTG CAAGCTGCTG GTCAAGGAGC 3120 TGCGCATGTG CCTTTCCTTT GATTCCAACT ACTGTCGCAA TATCCTCAAA CACGCCGTGG 3180 AAAACGGTGA CTCGGCCGAC ACGCTGCTGG AGCTGCTCAT CGAGGACTTT GACATCTACG 3240 TGGACAGCTT CCCGCAGTCG GCGCACACCT TTTTGGGCGC GCGCCCGCCG TCGTTGGAGT 3300 TTGACGATGA CGCCAATCTC CTCTCGCTCG GCGGCGGTTC AGCCTTCTCG TCGGTACCCA 3360 AGAAACATGT CCCCACGCAG CCGCTGGACG GCTGGAGCTG GATCGCCAGT CCCTGGAAGG 3420 GACACAAACC GTTCCGCTTC GAGGCCCATG GTTCTCTGGC ACCGGCCGCC GACGCCCACG 3480 CCGCCCGTTC GGCGCGCGTC GGCTATTACG ACGAAGAGGA AAAGCGTCGC GAGCGGCAGA 3540 AACGGGTGGA CGACGAGGTG GTGCAGCGTG AGAAACAGCA GCTGAAGGCT TGGGAGGAGA 3600 GGCAGCAGAA CCTGCAGCAA CGTCAGCAGC AACCGCCGCC CCCGACACGT AAACCGGGCG 3660 CCTCCCGGAG GCTCTTTGGC TCCAGTGCCG ATGAGGACGA CGACGATGAT GATGACGAGA 3720 AAAACATCTT TACGCCCATC AAGAAACCGG GAACTAGCGG CAAGGGCGCC GCTAGTGGCA 3780 ACGGTGTTTC CAGCATTTTC AGCGGCATGT TATCCTCGGG CAGTCAGAAA CCGACCAGCG 3840 GTCCCTTGAA CATCCCGCAG CAACAACAGC GTCACGCGGC TTTCAGTCTC GTCTCCCCGC 3900 AGGTAACCAA GGCCAGCCCG GGAAGGGTCC GTCGGGACAG CGCGTGGGAC GTGAGGCCGC 3960 TCACGGAGAC AAGAGGGGAT CTTTTCTCGG GCGACGAGGA TTCCGACAGC TCGGATGGCT 4020 ATCCCCCCAA CCGTCAAGAT CCGCGTTTCA CCGACACGCT GGTGGACATC ACGGATACCG 4080 AGACGAGCGC CAAACCGCCC GTCACCACCG CGTACAAGTT CGAGCAACCG ACGTTGACGT 4140 TCGGCGCCGG AGTTAACGTC CCTGCTGGCG CCGGCGCTGC CATCCTCACG CCGACGCCTG 4200 TCAATCCTTC CACGGCCCCC GCTCCGGCCC CGACACCTAC CTTCGCGGGT ACCCAAACCC 4260 CGGTCAACGG TAACTCGCCC TGGGCTCCGA CGGCGCCGTT GCCCGGGGAT ATGAACCCCG 4320 CCAACTGGCC GCGCGAACGC GCGTGGGCCC TCAAGAATCC TCACCTGGCT TACAATCCCT 4380 TCAGGATGCC TACGACTTCC ACGACTTCTC AAAACAACGT GTCCACCACC CCTCGGAGGC 4440 CGTCGACTCC ACGCGCCGCG GTGACACAAA CAGCGTCTCA GAACGCCGCT GATGAGGTTT 4500 GGGCTTTAAG GGACCAAACT GCAGAGTCAC CGGTCGAAGA CAGCGAGGAG GAAGACGACG 4560 ACTCCTCGGA CACCGGCTCC GTCGTCAGCC TGGGACACAC AACACCGTCG TCCGATTACA 4620 ACGACGTCAT TTCGCCTCCC AGTCAGACGC CCGAGCAGTC GACGCCGTCC AGAATACGTA 4680 AAGCTAAGTT ATCGTCTCCA ATGACGACGA CATCCACGAG CCAGAAACCG GTGCTGGGCA 4740 AGCGAGTCGC GACGCCGCAC GCGTCCGCCC GAGCGCAGAC GGTGACGTCG ACACCGGTTC 4800 AGGGAAGGGT AGAGAAACAG GTATCGGGCA CGCCGTCGAC GGTACCCGCC ACGCTGTTGC 4860 AACCTCAACC GGCTTCGTCT AAAACAACGT TATCAAGGAA CGTGACTTCT GGCGCGAGAA 4920 CCTCTTCCGC TTCGGCTCGA CAGCCGTCAG CCTCGGCGTC CGTTTTGTCG CCCACGGAGG 4980 ATGATGTCGT GTCCCCCGTC ACGTCGCCGC TGTCCATGCT TTCGTCAGCC TCTCCGTCCC 5040 CGGCCAAGAG TGCCCCTCCG TCTCCGGTGA AAGGTCGGGG CAGCCGCGTC GGTGTTCCTT 5100 CTTTGAAACC TACTTTGGGC GGCAAGGCGG TGGTAGGTCG ACCGCCCTCG GTACCCGTGA 5160 GCGGTAGCGC GCCGGGTCGC CTGTCCGGCA CCAGCCGGGC CGCCTCGACC ACGCCGACGT 5220 ATCCCGCGGT AACCACCGTT TACCCACCGT CGTCTACGGC CAAAAGCAGC GTATCGAATG 5280 CGCCGCCTGT GGCCTCCCCC TCCATCCTGA AACCGGGGGC GAGCGCGGCT TTGCAATCAC 5340 GCCGCTCGAC GGGGACCGCC GCCGTAGGTT CCCCCGTCAA GAGCACGACG GGCATGAAAA 5400 CGGTGGCTTT CGACCTATCG TCGCCCCAGA AGAGCGGTAC GGGGCCGCAA CCGGGTTCTG 5460 CCGGCATGGG GGGCGCCAAA ACGCCGTCGG ACGCCGTGCA GAACATCCTC CAAAAGATCG 5520 AGAAGATTAA GAACACGGAG GAATAGTTTT TATTGCTAGA ATTCTTTTTA TTGATTAACT 5580 AGTCAAATGA GTATATATAA TTGAAAAAGT AAAATATAAA TCATATAATA ATGAAACGAA 5640 ATATCAGTAA TAGACAGGAA CTGGCAGATT CTTCTTCTAA TGAAGTAAGT ACTGCTAAAT 5700 CTCCAAAATT AGATAAAAAT GATACAGCAA ATACAGCTTC ATTCAACGAA TTACCTTTTA 5760 ATTTTTTCAG ACACACCTTA TTACAAACTA ACTAAGTCAG ATGATGAGAA AGTAAATATA 5820 AATTTAACTT ATGGGTATAA TATAATAAAG ATTCATGATA TTAATAATTT ACTTAACGAT 5880 GTTAATAGAC TTATTCCATC AACCCCTTCA AACCTTTCTG GATATTATAA AATACCAGTT 5940 AATGATATTA AAATAGATTG TTTAAGAGAT GTAAATAATT ATTTGGAGGT AAAGGATATA 6000 AAATTAGTCT ATCTTTCACA TGGAAATGAA TTACCTAATA TTAATAATTA TGATAGGAAT 6060 TTTTTAGGAT TTACAGCTGT TATATGTATC AACAATACAG GCAGATCTAT GGTTATGGTA 6120 AAACACTGTA ACGGGAAGCA GCATTCTATG GTAACTGGCC TATGTTTAAT AGCCAGATCA 6180 TTTTACTCTA TAAACATTTT ACCACAAATA ATAGGATCCT CTAGATATTT AATATTATAT 6240 CTAACAACAA CAAAAAAATT TAACGATGTA TGGCCAGAAG TATTTTCTAC TAATAAAGAT 6300 AAAGATAGTC TATCTTATCT ACAAGATATG AAAGAAGATA ATCATTTAGT AGTAGCTACT 6360 AATATGGAAA GAAATGTATA CAAAAACGTG GAAGCTTTTA TATTAAATAG CATATTACTA 6420 GAAGATTTAA AATCTAGACT TAGTATAACA AAACAGTTAA ATGCCAATAT CGATTCTATA 6480 TTTCATCATA ACAGTAGTAC ATTAATCAGT GATATACTGA AACGATCTAC AGACTCAACT 6540 ATGCAAGGAA TAAGCAATAT GCCAATTATG TCTAATATTT TAACTTTAGA ACTAAAACGT 6600 TCTACCAATA CTAAAAATAG GATACGTGAT AGGCTGTTAA AAGCTGCAAT AAATAGTAAG 6660 GATGTAGAAG AAATACTTTG TTCTATACCT TCGGAGGAAA GAACTTTAGA ACAACTTAAG 6720 TTTAATCAAA CTTGTATTTA TGAAGGTAC 6749 5798 base pairs nucleic acid single linear DNA (genomic) unknown 39 TCTAGAACTA GTGGATCTTC TGGTAATGAC AAATTAAACT GTTTAGCGTA TATTATATAC 60 TCGTATAAAA AATCATGATC TATATTCTTA ATAGCTTTTA GAAGGTTCAT ATCGTAGAAA 120 TAAACATAAG TTCCTTTCAT CACTCTACCT ACACGACCTT TACGTTGCGT CATCATAGAT 180 TTTGATATAA ACATCTGAAC ACCACCAAAA GGTCTAGGTA CGTATACTCT ACCGGTATCG 240 TATACGTGAG TCGCTGTACG TATAGTAATA CTAGATTCCA AATAAGGGGT AGATACTAGA 300 ATACAAGGTC TTTCTCTATT AGGTCGTTGA ACATCTTGTA GGATTTCTGC TATATTTTTT 360 AATTTTCCAT GTATTACTAT AAAATCAATA TTCTTATTCT TAGATTCTAA GTACTCTTTA 420 TACTTAATAC ATTCTGATAC AGAAGGTAAG AATAAAATAC CACACATTCC ATTATCTGGC 480 TTACACCACA ATAAAGTAGA CGATATATTC TTTCTCTCAT TATCAAAATA AACTCTCTTA 540 TCCGGAGAAT ACCTATTTTT TACGTATATT TCTTTTATGG AGTAAAGAAC TGGTCCTTCT 600 ATATGGTAAA ATTCAACATC AGGAAGAAAT TCCATTAGTC TATCTTTATC ATCTTCTAGA 660 GTGGCAGACA TCAATACTAG CGAATGAATG CTATCTATAT TTTTTCTTAG AACGGCTATC 720 ATAATATCGG CTATCCTATC ATGTTCATGT ATTTCATCTA TTATGACTAT ATTATACTTT 780 GATAGAGAGT AACTAGTCAG TTTATTAGTA GAAAGTACTA TACCTTGAAA TCCTTTTTTG 840 GTTTTTTCTG TATGTCCTCC GTATTTAAGT TCTACAGGAG AACCTTCGAA CTGTGAAAAT 900 CCCAACGATT GTAAAAAATT ATTTCCGTTG CTCTTTACCA AAGTCACCCT AGGAAGAGAT 960 AAAACTATAG GTTTGGGTAT AAAATCTAGC CTTATCCTGT CTATATCATC CCATCCTCCG 1020 AATAAATAGT TATACCACAT TATTACTTTT GGTAACTGAG ATGTTTTACC TATGCCTGTA 1080 CTACCGGTAA CTACTATCTG TTTCCTCTTC TTTAACATAT CAAAGATATG AACCTGTGTT 1140 GTTAAACTAA GGGATTTGAA CGATATGATA GCGAAAGGAT TTGGATTATT GAGTATTCCT 1200 ATAGAATTCT TAATGGGTAC CTTCTTATTG GAAGAGAAAA TAGACAGATG ATTTCCAGCT 1260 ACTAGTAATC CTCTTTTATC GTCAAGCGTT ATATCAGATA CATGATTATA ACCGATACAT 1320 TTTACGTAAC TATAGCATTC AAACGTTATA AATCTATCGT TACCTATATA GTATACCTGT 1380 TTACTGTAGT TGATACTGAC GGGTATTATA TCTATAAGTT TACTAACAGG TATTTTAGCG 1440 GGTATTGAAT TAGTAGTTTC TATATTCAGC ATATAAGTAT CGTCCTTTAA GCAGATAAAT 1500 ACTTTATTCC ACCTATGTTT TATTATAGGA AATACAGAAT GAGAAAAAAA TAACGTATCT 1560 TTATTATGAT ATTCTTCTAA TTCTTTTTGG GTATACTTAC TTGGGAATAT ATCGTACATA 1620 TTAGGGAAAG CGTATATCGA AAATAGCTCG TTAGTGGCCA TAGTTCCTAC AGTATGTATA 1680 TTTAGTTAGT AATAAATGGA TAGATACACA GAACTAGTTA TTAATAAAAT ACCAGAATTA 1740 GGATTCGTTA ACTTGCTTTC TCATATCTAT CAAACAGTTG GGTTATCCTA CGATATAGAT 1800 GTATCAAAAT TCAAAACTAA TTGCAATGGT TACGTCGTAG AGAGATTTGA TAACTCAGAA 1860 ACAGTTGGCA AAGTGTCCTG CGTGCCTATA TCTATACTGT TAGAATTGGT AGACAGAAAA 1920 ATATTATCTA AACCAGATAC GTCTAAAACA GAAATAGAGA TTAAAGAAGA TTTAGTAAAC 1980 GAATTAATTG AAAATACCAA TAGTTTCGAA GATATAATGA CTATACCTAC CAGTATCCCT 2040 ATGAGATATT TTTTTAAACC GGTACTAAGA GAAAAAGTAT CTAAAGCTGT AGATTTTTCC 2100 AGAATGGATA TTAAGGGAGA TGATATTAGC AAAATGGGAA TAAAACACGG AGAAAAAAGT 2160 AATAATATAT CTAATATTAA GATTGTACCA GAAAAAGATG CCTGGATGAC TAATACTAGT 2220 ATTCAGCAAT TAATAGGACC TATGTCGTAC GGAACAGAAG TTAGCTATAT AGGTCAATTT 2280 AACTTTAATT TTATTAACAC ATATCCTGTA TACGAAAAAT CTGCAGCCCT TAACAGAAGT 2340 CCAGAACTTT TTAAGATTAA AGATAGAATT AAAGGATTAC GTACAAGATT TGTTATGTTC 2400 GGTTTCTGTT ATATGTTCCA TTGGAAATGT TTGATATATG ATAGAGAAAA CGATTTTGTA 2460 TGTTTCTATG ATTCAGGAGG ATCTAATCCA AATGACTTTG ATCACTATGA TAATTTTTTC 2520 TACTATAGTC ATTCGAGAGG ATTCAATAGA AATTCTAAGA GGTCATCTAG CTTATCTAAT 2580 GAAAATGCAG ATATAGATAT TCTGTTCAAC TTTTTCGTGG ATAATTACGA AGTTACTTCA 2640 GGATGTATAA ACGTAGAAGT CAATCAGCTG ATGGAATCAG AATGTGGTAT GTTTACTTGT 2700 TTGTTTATGA CTATGTGCTG TCTCCATCCT CCTAAAGGAT TTAAAGGGAT AAGAAAGACA 2760 TATACCTATT TTAAGTTTTT AGCCGATAAA AAAATGACTA TGCTAAAGTC TATACTTTTC 2820 AACGCTGACA AGATGGAATT TAAAGTGAAA GAATCAAGCA GTAAAGGCAT ACAAGAATAT 2880 AAAAAAATGG AAGAGTGGTG TGGTAAAACT ATAAACATTT TAGCTGATAA AATAACAACA 2940 CGTGTAAATA GTATAATAGA GTAGTAAAAT GGATAATTTT ATAAAGCAGA TATCGTCAAA 3000 GATAGTAAAA CCTATAGCAG AATTAGAACC TCCAGATTCT AAAGTACAAT ATTATTACAT 3060 GACTATATCG TTTAATTTTC CTGACTTATA TTATTGTAAT AAAAATTTAT TTGCGAAACC 3120 CGATAATACT TTGCTAGATG TTTCTAAGTC TTTGCTTACT TTAAACTCAT TTCCGTATGA 3180 AAACTTTGTG ATAAATGATT TACTAAGAAC TATTAGGCGT TACTGTCACG TATATGATGT 3240 CTATTTTTTA CCCGTAGGGT GGTTTGTAGG AAAAGAAGAT GTATTACCCA ATTACCAAGT 3300 ATCGATAAAA ATAATAAGAA GTACTAATCA AGAAGTAATA GAAAACATTA TTAGGAATTA 3360 TTTATCACGA CACGGTATTT ATGGAGATAA CCTATCTATA GAAACAGACC GATTAAACGA 3420 AGTATCTATA AACAGACATT CTATTGTAGG AGCTAGACAG TTAGCACCTA TATGCGTTGT 3480 TTCTTTTTAT CCTTTCGACC CTGAAAATAA AATACTTTTC GTTATATATG TAGGTAGATA 3540 CAAAGACAGA CATTGCGGTG TATCTTATGT AGTTGATAGA GAGGATATGT ATAAAGTAAT 3600 TAACAGAATA TATTCTTACG TAGTTTGTAT TTATCTAGTT TCCGATGATA TGGTCACGTT 3660 TCATACTACT CCTCTAGCTA ATCACAGTAA AAAATTAATA CCGTTACCCA TAAATCATTG 3720 CAATACCTTA TGCGAGATAG TTCACGACTT TGAGTTTTTA AGATTTGAGC AATCCACTAT 3780 GCCAATACCC GTTTTCACTC CTTTTATTCC TAAACAGCTA GTTAATATAA TCAACTTACC 3840 TGATGATATA CCTATTACTT GTGCATCAAT AAACAGATTA GAATATGTTA CACATATAGA 3900 TGATAAAAAA TTAAAAAGAG TACTGATTAT CGTAAAGGAT AAATTTCTTA GAAATACTAT 3960 TCTTCACGGT ACATTTAAAA AAAGGAATAT AGTCAGAAAC AGGAAATATA CTTTCACTAT 4020 AACATGGTCT AATTTCGAAT GTCCGACGTT AGGAGACGTT AAGTCTTCTT CACCTAATAC 4080 CTGTAATAGA GTAGTTTTAG ACGGTAGTAG ATACGTTACA AAAACCTTTA ATGATACAAT 4140 ATAAATGGAA CTAACTAGAG AAACGCTGAT ATTTGTAGGC ATTACTGTAC TAGTAGTAGT 4200 AATGATCATA TCTGGTTTCT CACTAATATT GCGATTGATA CCTGGTGTAT ATTCATCAGT 4260 TATTAGATCG TCGTTCGTAG GAGGGAAAAT ATTAAGATTT ATGGAGGTAT TCTCTACTGT 4320 TATGTTTATA CCATCATTAG TAATACTTTA TACAGCATAT ATAAGGAAAT CTAAAGTGAA 4380 AAATAACTAA ATATTATAGT ATTTGTAATA AATGGCTACT GGAGAGATTC GTCTTATTAT 4440 AGGGCCTATG TTTTCAGGTA AAACAACAGA ATTAGTTAGA TTAATAAGAA GATTTATGAT 4500 ATCGGGACGT AAATGTATAA TAATAAAACA TTGTAGTGAT TCCCGTTATA CCGAAGGAGA 4560 TTTAGAAGCT ATATATACTC ATGATAAAAT TTCGATGGAA GCACTATCGT GTAGCAAATT 4620 ATTACCTTTA ATACCTAAAA TTGATAACTT TGAAGTAATA GGTATAGACG AAGGACAGTT 4680 TTTTGAAGAT ATAGTAGAAT TTAGTGAGAT TATGGCTAAT AAGGGTAAAA CTGTAATCAT 4740 AGCGGCTTTA AATGGAGATT TCAAACGACA ATTATTTGGA AACATATTTA AACTATTATC 4800 TTTATCAGAA TCAGTTACTA GTTTAACTGC TATTTGTGCA GTTTGTAAAA ACGAAGCATC 4860 TTTTTCTAAG CGCATGACTG ATGATAAAGA TGTAAAAGTT ATAGGAGGTA AAGAAATGTA 4920 TACTGCTGTT TGTAGAAAAT GCTTTTTATG AGTCTAATAT ACGTACTAAA TACTTGTACG 4980 TACAACTATG TTAGAATAAT TTGCTTAGTA TAGTATATAA ACAAGTATGT AAAAAATAAA 5040 ATTGATATAA AAGTAGTCTT CTATTCCGAA CAATAACTAT ACAAAATGGA TTTAGATATT 5100 AAATCTTGCA GAAGTATTTA CAAAATATGG GATAAATATC ATTTTATGAC AGGGTATAAA 5160 TATAAAAATG ATAAACAGAG ATTTAAAATT ACAATTTACT GTAAATGTGA TTGTTCTATC 5220 AAAGAATATC CTTATAGATT TGTTACTGAG AAACTGCTTT TAATGTATAT TATTAATAAG 5280 TTTAGAGGAA AGTATCTAAT CAAAATTAGG ATAGAACCCA TAGTTAAAAA TTAAATCATA 5340 TATCAATACA TGTCAGTTTT TTATCGAAAA ATGGATTTAT AAATAAAATG AAAAATAACT 5400 TGAATGAAGG AAAAAATAAC CATGAGTAAA AAACCAGTAA AGACGGTCCA GCGTAGACGT 5460 GGAAACGATG AGGATAATAA GTTTACTTGT ATCCAAGCGC TAGAACATGC AAAAAGCTTA 5520 TGTACTAAAA ATAATAAAAT AGTTAAATCT GTTAAACTAT CACAATCTCT CTTTAAGTCA 5580 TCTAACAATA TTTCTGTGAT ATTAGAACCA GAATATAAAG ACAAATTAGT GACTCCTCTT 5640 ATTATTGTAG AAGGTGAAGG AAAAATATAC CATAATAAGA ATGATAGTTT TAATCGTGAA 5700 GAACCGTATT TTCTAAAAAT ACGACCTACG TTAATGAATC CTATATTATA TCAGATTATG 5760 GAATGCATTT ATAGAGATCC CCCGGGCTGC AGGAATTC 5798 5302 base pairs nucleic acid single linear DNA (genomic) unknown 40 GCCCTTAACA GAAGTCCAGA ACTTTTTAAG ATTAAAGATA GAATTAAAGG ATTACGTACA 60 AGATTTGTTA TGTTCGGTTT CTGTTATATG TTCCATTGGA AATGTTTGAT ATATGATAGA 120 GAAAACGATT TTGTATGTTT CTATGATTCA GGAGGATCTA ATCCAAATGA CTTTGATCAC 180 TATGATAATT TTTTCTACTA TAGTCATTCG AGAGGATTCA ATAGAAATTC TAAGAGGTCA 240 TCTAGCTTAT CTAATGAAAA TGCAGATATA GATATTCTGT TCAACTTTTT CGTGGATAAT 300 TACGAAGTTA CTTCAGGATG TATAAACGTA GAAGTCAATC AGCTGATGGA ATCAGAATGT 360 GGTATGTTTA CTTGTTTGTT TATGACTATG TGCTGTCTCC ATCCTCCTAA AGGATTTAAA 420 GGGATAAGAA AGACATATAC CTATTTTAAG TTTTTAGCCG ATAAAAAAAT GACTATGCTA 480 AAGTCTATAC TTTTCAACGC TGACAAGATG GAATTTAAAG TGAAAGAATC AAGCAGTAAA 540 GGCATACAAG AATATAAAAA AATGGAAGAG TGGTGTGGTA AAACTATAAA CATTTTAGCT 600 GATAAAATAA CAACACGTGT AAATAGTATA ATAGAGTAGT AAAATGGATA ATTTTATAAA 660 GCAGATATCG TCAAAGATAG TAAAACCTAT AGCAGAATTA GAACCTCCAG ATTCTAAAGT 720 ACAATATTAT TACATGACTA TATCGTTTAA TTTTCCTGAC TTATATTATT GTAATAAAAA 780 TTTATTTGCG AAACCCGATA ATACTTTGCT AGATGTTTCT AAGTCTTTGC TTACTTTAAA 840 CTCATTTCCG TATGAAAACT TTGTGATAAA TGATTTACTA AGAACTATTA GGCGTTACTG 900 TCACGTATAT GATGTCTATT TTTTACCCGT AGGTGGTTTG TAGGAAAAGA AGATGTATTA 960 CCCAATTACC AAGTATCGAT AAAAATAATA AGAAGTACTA ATCAAGAAGT AATAGAAAAC 1020 ATTATTAGGA ATTATTTATC ACGACACGGT ATTTATGGAG ATAACCTATC TATAGAAACA 1080 GACCGATTAA ACGAAGTATC TATAAACAGA CATTCTATTG TAGGAGCTAG ACAGTTAGCA 1140 CCTATATGCG TTGTTTCTTT TTATCCTTTC GACCCTGAAA ATAAAATACT TTTCGTTATA 1200 TATGTAGGTA GATACAAAGA CAGACATTGC GGTGTATCTT ATGTAGTTGA TAGAGAGGAT 1260 ATGTATAAAG TAATTAACAG AATATATTCT TACGTAGTTT GTATTTATCT AGTTTCCGAT 1320 GATATGGTCA CGTTTCATAC TACTCCTCTA GCTAATCACA GTAAAAAATT AATACCGTTA 1380 CCCATAAATC ATTGCAATAC CTTATGCGAG ATAGTTCACG ACTTTGAGTT TTTGAGATTT 1440 GAGCAATCCA CTATGCCAAT ACCCGTTTTC ACTCCTTTTA TTCCTAAACA GCTAGTTAAT 1500 ATAATCAACT TACCTGATGA TATACCTATT ACTTGTGCAT CAATAAACAG ATTAGAATAT 1560 GTTACACATA TAGATGATAA AAAATTAAAA AGAGTACTGA TTATCGTAAA GGATAAATTT 1620 CTTAGAAATA CTATTCTTCA CGGTACATTT AAAAAAAGGA ATATAGTCAG AAACAGGAAA 1680 TATACTTTCA CTATAACATG GTCTAATTTC GAATGTCCGA CGTTAGGAGA CGTTAAGTCT 1740 TCTTCACCTA ATACCTGTAA TAGAGTAGTT TTAGACGGTA GTAGATACGT TACAAAAACC 1800 TTTAATGATA CAATATAAAT GGAACTAACT AGAGAAACGC TGATATTTGT AGGCATTACT 1860 GTACTAGTAG TAGTAATGAT CATATCTGGT TTCTCACTAA TATTGCGATT GATACCTGGT 1920 GTATATTCAT CAGTTATTAG ATCGTCGTTC GTAGGAGGGA AAATATTAAG ATTTATGGAG 1980 GTATTCTCTA CTGTTATGTT TATACCATCA TTAGTAATAC TTTATACAGC ATATATAAGG 2040 AAATCTAAAG TGAAAAATAA CTAAATATTA TAGTATTTGT AATAAGTACT AATTAGCTAT 2100 AAAAACCCGG GCTCGAGATA AAAATTACTG GTCAGCCTTG CTTCTAGTCA CCATAGGGTG 2160 GGTACTCTTA CCTCCAGAGG CGGTGGGTTC CTCAGCACCA TCCTCCTCTT CCTCTGGGGC 2220 AACTTCCTCT ATCTCAGACA CTGGCTCAGA CTTGACAGAC ACAGTGTCCT CCCGCTCCTC 2280 CTGAGCACCC TCCTCCTCTT CCTCATCACT CTGCTCACTT TCTTCCTGAT CACTGTTCTC 2340 AGCCACAATT ACTGAGGACA GAGGGATAGT CGCGGGTACA GGGGACTCTG GGGGTGACAC 2400 CAGAGAATCA GAGGAGCTGA CACCAGCGGT GGCCAAAGTG TAGGCTACAA TAGCCTCTTC 2460 CTCATCTGAC TCCTCGGCGA TGGCCCGTAG GTCATCCACA CTAGGAGAGC AGACTCTCAG 2520 AGGATCGGCC CCCAGAATGT ACTGGGCAAA GACCTTCATG CAGATCTCCT CAATGCGGCG 2580 CTTCATTACA CTGATAACCT CAGGCTTGGT TATCAGAGGC CGCTTGGCCA GCATCACACT 2640 AGTCTCCTCT AAGACATAGC AGCACAGCAC CCGACAGAAC TCACTTAAGA GAGAGATGCC 2700 CCCGTACATG GTCATCATAC AAGCGTCACT AGTGACCTTG TACTCATTAC ACATTGTTTC 2760 CACACATGTA GTGAGGATAT CCATAAATAT GTGATCAATG TGCGTGAGCA CCTTGTCTCT 2820 CTCCTCATCC AAAATCTTAA ATATTTTCTG GGCATAAGCC ATAATCTCAT CAGGGGAGCA 2880 CTGAGGCAAG TTCTGCAGTG CCGCCATGGC CTGACTGCAG CCATTGGTGG TCTTAGGGAA 2940 GGCTGAGTTC TTGGTAAACA ACTCTATATT CCTGTAGCAC ATATACATCA TCTTTCTCCT 3000 AAGTTCATCC TTTTTAGCAC GGGCCTTAGC CTGCAGTGCA CCCCCCAACT TGTTAGCGGC 3060 GCCCTTGCTC ACATCATGCA GCTCCTTAAT ACAAGCCATC CACATCTCCC GCTTATCCTC 3120 AGGTACAATG TAGTTCTCAT ACATGCTCTG CATAGTTAGC CCAATACACT TCATCTCCTC 3180 GAAAGGCTCA TGAACCTTAT CTAAGATATC TAAGGCATTC TGCAAACATC CTCCCATCAT 3240 ATTAAAGGCG CCAGTGAATT TCTCTTCCGT CTGGGTATAT TTTTTCAGCA TGTGCTCCTT 3300 GATTCTATGC CGCACCATGT CCACTCGAAC CTTAATCTGT TTCATTACGA TACAAACTTA 3360 ACGGATATCG CGATAATGAA ATAATTTATG ATTATTTCTC GCTTTCAATT TAACACAACC 3420 CTCAAGAACC TTTGTATTTA TTTTCACTTT TTAAGTATAG AATAAAGAAG GATCCTTCTT 3480 TATTCTATAC TTAAAAAGTG AAAATAAATA CAAAGGTTCT TGAGGGTTGT GTTAAATTGA 3540 AAGCGAGAAA TAATCATAAA TTATTTCATT ATCGCGATAT CCGTTAAGTT TGTATCGTAA 3600 TGTGCCGCCG CCCGGATTGC GGCTTCTCTT TCTCACCTGG ACCGGTGGCA CTGCTGTGGT 3660 GTTGCCTTCT GCTGCCCATC GTTTCCTCAG CCACCGTCAG CGTCGCTCCT ACCGTCGCCG 3720 AGAAAGTTCC CGCGGAGTGC CCCGAACTAA CGCGTCGATG CCTGTTGGGT GAGGTGTTTC 3780 AGGGTGACAA GTATGAAAGT TGGCTGCGCC CGTTGGTGAA TGTTACCAGA CGCGATGGCC 3840 CGCTATCGCA ACTTATTCGT TACCGTCCCG TTACGCCGGA GGCCGCCAAC TCCGTGCTGT 3900 TGGACGATGC TTTCCTGGAC ACTCTGGCCC TGCTGTACAA CAATCCGGAT CAATTGCGGG 3960 CCTTGCTGAC GCTGTTGAGC TCGGACACAG CGCCGCGCTG GATGACGGTG ATGCGCGGTT 4020 ACAGCGAGTG CGGCGATGGC TCGCCGGCCG TGTACACGTG CGTGGACGAC CTGTGCCGCG 4080 GCTACGACCT CACGCGACTG TCATACGGGC GCAGCATCTT CACGGAACAC GTGTTAGGCT 4140 TCGAGCTGGT GCCACCGTCT CTCTTTAACG TGGTGGTGGC CATACGCAAC GAAGCCACGC 4200 GTACCAACCG CGCCGTGCGT CTGCCCGTGA GCACCGCTGC CGCGCCCGAG GGCATCACGC 4260 TCTTTTACGG CCTGTACAAC GCAGTGAAGG AATTCTGCCT GCGTCACCAG CTGGACCCGC 4320 CGCTGCTACG CCACCTAGAT AAATACTACG CCGGACTGCC GCCCGAGCTG AAGCAGACGC 4380 GCGTCAACCT GCCGGCTCAC TCGCGCTATG GCCCTCAAGC AGTGGATGCT CGCTAATTTT 4440 TATAGATCCC TCGAGGGTAC CGCATGCCCT TTTTATTGAC TAGTTAATCA GTCTAATATA 4500 CGTACTAAAT ACTTGTACGT ACAACTATGT TAGAATAATT TGCTTAGTAT AGTATATAAA 4560 CAAGTATGTA AAAAATAAAA TTGATATAAA AGTAGTCTTC TATTCCGAAC AATAACTATA 4620 CAAAATGGAT TTAGATATTA AATCTTGCAG AAGTATTTAC AAAATATGGG ATAAATATCA 4680 TTTTATGACA GGGTATAAAT ATAAAAATGA TAAACAGAGA TTTAAAATTA CAATTTACTG 4740 TAAATGTGAT TGTTCTATCA AAGAATATCC TTATAGATTT GTTACTGAGA AACTGCTTTT 4800 AATGTATATT ATTAATAAGT TTAGAGGAAA GTATCTAATC AAAATTAGGA TAGAACCCAT 4860 AGTTAAAAAT TAAATCATAT ATCAATACAT GTCAGTTTTT TATCGAAAAA TGGATTTATA 4920 AATAAAATGA AAAATAACTT GAATGAAGGA AAAAATAACC ATGAGTAAAA AACCAGTAAA 4980 GACGGTCCAG CGTAGACGTG GAAACGATGA GGATAATAAG TTTACTTGTA TCCAAGCGCT 5040 AGAACATGCA AAAAGCTTAT GTACTAAAAA TAATAAAATA GTTAAATCTG TTAAACTATC 5100 ACAATCTCTC TTTAAGTCAT CTAACAATAT TTCTGTGATA TTAGAACCAG AATATAAAGA 5160 CAAATTAGTG ACTCCTCTTA TTATTGTAGA AGGTGAAGGA AAAATATACC ATAATAAGAA 5220 TGATAGTTTT AATCGTGAAG AACCGTATTT TCTAAAAATA CGACCTACGT TAATGAATCC 5280 TATATTATAT CAGATTATGG AA 5302 2151 base pairs nucleic acid single linear DNA (genomic) unknown 41 ATGCGGCCAG GCCTCCCCTC CTACCTCATC GTCCTCGCCG TCTGTCTCCT CAGCCACCTA 60 CTTTCGTCAC GATATGGCGC AGAAGCCATA TCCGAACCGC TGGACAAAGC GTTTCACCTA 120 CTGCTCAACA CCTACGGGAG ACCCATCCGC TTCCTGCGTG AAAACACCAC CCAGTGTACC 180 TACAATAGCA GCCTCCGTAA CAGCACGGTC GTCAGGGAAA ACGCCATCAG TTTCAACTTT 240 TTCCAAAGCT ATAATCAATA CTATGTATTC CATATGCCTC GATGTCTTTT TGCGGGTCCT 300 CTGGCGGAGC AGTTTCTGAA CCAGGTAGAT CTGACCGAAA CCCTGGAAAG ATACCAACAG 360 AGACTTAACA CTTACGCGCT GGTATCCAAA GACCTGGCCA GCTACCGATC TTTTTCGCAG 420 CAGCTAAAGG CACAGGACAG CCTAGGTGAA CAGCCCACCA CTGTGCCACC ACCCATTGAC 480 CTGTCAATAC CTCACGTTTG GATGCCACCG CAAACCACTC CACACGGCTG GACAGAATCA 540 CATACCACCT CAGGACTACA CCGACCACAC TTTAACCAGA CCTGTATCCT CTTTGATGGA 600 CACGATCTAC TATTCAGCAC CGTCACACCT TGTTTGCACC AAGGCTTTTA CCTCATCGAC 660 GAACTACGTT ACGTTAAAAT AACACTGACC GAGGACTTCT TCGTAGTTAC GGTGTCCATA 720 GACGACGACA CACCCATGCT GCTTATCTTC GGCCATCTTC CACGCGTACT CTTTAAAGCG 780 CCCTATCAAC GCGACAACTT TATACTACGA CAAACTGAAA AACACGAGCT CCTGGTGCTA 840 GTTAAGAAAG ATCAACTGAA CCGTCACTCT TATCTCAAAG ACCCGGACTT TCTTGACGCC 900 GCACTTGACT TCAACTACCT GGACCTCAGC GCACTACTAC GTAACAGCTT TCACCGTTAC 960 GCCGTGGATG TACTCAAAAG CGGTCGATGT CAGATGCTGG ACCGCCGCAC GGTAGAAATG 1020 GCCTTCGCCT ACGCATTAGC ACTGTTCGCA GCAGCCCGAC AAGAAGAGGC CGGCGCCCAA 1080 GTCTCCGTCC CACGGGCCCT AGACCGCCAG GCCGCACTCT TACAAATACA AGAATTTATG 1140 ATCACCTGCC TCTCACAAAC ACCACCACGC ACCACGTTGC TGCTGTATCC CACGGCCGTG 1200 GACCTGGCCA AACGAGCCCT TTGGACACCG AATCAGATCA CCGACATCAC CAGCCTCGTA 1260 CGCCTGGTCT ACATACTCTC TAAACAGAAT CAGCAACATC TCATCCCCCA GTGGGCACTA 1320 CGACAGATCG CCGACTTTGC CCTAAAACTA CACAAAACGC ACCTGGCCTC TTTTCTTTCA 1380 GCCTTCGCGC GTCAAGAACT CTACCTCATG GGCAGCCTCG TCCACTCCAT GCTAGTACAT 1440 ACGACGGAGA GACGCGAAAT CTTCATCGTA GAAACGGGCC TCTGTTCATT AGCCGAGCTA 1500 TCACACTTTA CGCAGTTGCT AGCTCATCCG CACCACGAAT ACCTCAGCGA CCTGTACACA 1560 CCCTGTTCCA GTAGCGGGCG ACGCGATCAC TCGCTCGAAC GCCTCACACG TCTCTTCCCC 1620 GATGCCACCG TCCCCACTAC CGTTCCCGCC GCCCTCTCCA TCCTATCTAC CATGCAACCA 1680 AGCACGCTAG AAACCTTCCC CGACCTGTTT TGTCTGCCGC TCGGCGAATC CTTCTCCGCG 1740 CTGACCGTCT CCGAACACGT CAGTTATGTC GTAACAAACC AGTACCTGAT CAAAGGTATC 1800 TCCTACCCTG TCTCCACCAC CGTCGTAGGC CAGAGCCTCA TCATCACCCA GACGGACAGT 1860 CAAACTAAAT GCGAACTGAC GCGCAACATG CATACCACAC ACAGCATCAC AGCGGCGCTC 1920 AACATTTCCC TAGAAAACTG CGCCTTTTGC CAAAGCGCCC TACTAGAATA CGACGACACG 1980 CAAGGCGTCA TCAACATCAT GTACATGCAC GACTCGGACG ACGTCCTTTT CGCCCTGGAT 2040 CCCTACAACG AAGTGGTGGT CTCATCTCCG CGAACTCACT ACCTCATGCT TTTGAAAAAC 2100 GGTACGGTCC TAGAAGTAAC TGACGTCGTC GTGGACGCTA CCGACAGTCG T 2151 5062 base pairs nucleic acid single linear DNA (genomic) unknown 42 AAGCTTGCGG CCGCTCATTA GACAAGCGAA TGAGGGACGA AAACGTGGAG GAGGTATTAA 60 GTTTGGAGAA ATGGAGAGAG ACTGTTTAAT AGCGCATGGC GCAGCCAATA CTATTACAGA 120 AGTTTTGAAA GATTCGGAAG AAGATTATCA AGATGTGTAT GTTTGTGAAA ATTGTGGAGA 180 CATAGCAGCA CAAATCAAGG GTATTAATAC ATGTCTTAGA TGTTCAAAAC TTAATCTCTC 240 TCCTCTCTTA ACAAAAATTG ATACCACGCA CGTATCTAAA GTATTTCTTA CTCAAATGAA 300 CGCCAGAGGC GTAAAAGTCA AATTAGATTT CGAACGAAGG CCTCCTTCGT TTTATAAACC 360 ATTAGATAAA GTTGATCTCA AGCCGTCTTT TCTGGTGTAA TAAAAATTAA TTAATTACTC 420 GAGATAAAAA TCAACGACTG TCGGTAGCGT CCACGACGAC GTCAGTTACT TCTAGGACCG 480 TACCGTTTTT CAAAAGCATG AGGTAGTGAG TTCGCGGAGA TGAGACCACC ACTTCGTTGT 540 AGGGATCCAG GGCGAAAAGG ACGTCGTCCG AGTCGTGCAT GTACATGATG TTGATGACGC 600 CTTGCGTGTC GTCGTATTCT AGTAGGGCGC TTTGGCAAAA GGCGCAGTTT TCTAGGGAAA 660 TGTTGAGCGC CGCTGTGATG CTGTGTGTGG TATGCATGTT GCGCGTCAGT TCGCATTTAG 720 TTTGACTGTC CGTCTGGGTG ATGATGAGGC TCTGGCCTAC GACGGTGGTG GAGACAGGGT 780 AGGAGATACC TTTGATCAGG TACTGGTTTG TTACGACATA ACTGACGTGT TCGGAGACGG 840 TCAGCGCGGA GAAGGATTCG CCGAGCGGCA GACAAAACAG GTCGGGGAAG GTTTCTAGCG 900 TGCTTGGTTG CATGGTAGAT AGGATGGAGA GGGCGGCGGG AACGGTAGTG GGGACGGTGG 960 CATCGGGGAA GAGACGTGTG AGGCGTTCGA GCGAGTGATC GCGTCGCCCG CTACTGGAAC 1020 AGGGTGTGTA CAGGTCGCTG AGGTATTCGT GGTGCGGATG AGCTAGCAAC TGCGTAAAGT 1080 GTGATAGCTC GGCTAATGAA CAGAGGCCCG TTTCTACGAT GAAGATTTCG CGTCTCTCCG 1140 TCGTATGTAC TAGCATGGAG TGGACGAGGC TGCCCATGAG GTAGAGTTCT TGACGCGCGA 1200 AGGCTGAAAG AAAAGAGGCC AGGTGCGTTT TGTGTAGTTT TAGGGCAAAG TCGGCGATCT 1260 GTCGTAGTGC CCACTGGGGG ATGAGATGTT GCTGATTCTG TTTAGAGAGT ATGTAGACCA 1320 GGCGTACGAG GCTGGTGATG TCGGTGATCT GATTCGGTGT CCAAAGGGCT CGTTTGGCCA 1380 GGTCCACGGC CGTGGGATAC AGCAGCAACG TGGTGCGTGG TGGTGTTTGT GAGAGGCAGG 1440 TGATCATAAA TTCTTGTATT TGTAAGAGTG CGGCCTGGCG GTCTAGGGCC CGTGGGACGG 1500 AGACTTGGGC GCCGGCCTCT TCTTGTCGGG CTGCTGCGAA CAGTGCTAAT GCGTAGGCGA 1560 AGGCCATTTC TACCGTGCGG CGGTCCAGCA TCTGACATCG ACCGCTTTTG AGTACATCCA 1620 CGGCGTAACG GTGAAAGCTG TTACGTAGTA GTGCGCTGAG GTCCAGGTAG TTGAAGTCAA 1680 GTGCGGCGTC AAGAAAGTCC GGGTCTTTGA GATAAGAGTG ACGGTTCAGT TGATCTTTCT 1740 TAACTAGCAC CAGGAGCTCG TGTTTTTCAG TTTGTCGTAG TATAAAGTTG TCGCGTTGAT 1800 AGGGCGCTTT AAAGAGTACG CGTGGAAGAT GGCCGAAGAT AAGCAGCATG GGTGTGTCGT 1860 CGTCTATGGA CACCGTAACT ACGAAGAAGT CCTCGGTCAG TGTTATTTTA ACGTAACGTA 1920 GTTCGTCGAT GAGGTAAAAG CCTTGGTGCA AACAAGGTGT GACGGTGCTG AATAGTAGAT 1980 CGTGTCCATC AAAGAGGATA CAGGTCTGGT TAAAGTGTGG TCGGTGTAGT CCTGAGGTGG 2040 TATGTGATTC TGTCCAGCCG TGTGGAGTGG TTTGCGGTGG CATCCAAACG TGAGGTATTG 2100 ACAGGTCAAT GGGTGGTGGC ACAGTGGTGG GCTGTTCACC TAGGCTGTCC TGTGCCTTTA 2160 GCTGCTGCGA AAAAGATCGG TAGCTGGCCA GGTCTTTGGA TACCAGCGCG TAAGTGTTAA 2220 GTCTCTGTTG GTATCTTTCC AGGGTTTCGG TCAGATCTAC CTGGTTCAGA AACTGCTCCG 2280 CCAGAGGACC CGCAAAAAGA CATCGAGGCA TATGGAATAC ATAGTATTGA TTATAGCTTT 2340 GGAAAAAGTT GAAACTGATG GCGTTTTCCC TGACGACCGT GCTGTTACGG AGGCTGCTAT 2400 TGTAGGTACA CTGGGTGGTG TTTTCACGCA GGAAGCGGAT GGGTCTCCCG TAGGTGTTGA 2460 GCAGTAGGTG AAACGCTTTG TCCAGCGGTT CGGATATGGC TTCTGCGCCA TATCGTGACG 2520 AAAGTAGGTG GCTGAGGAGA CAGACGGCGA GGACGATGAG GTAGGAGGGG AGCCCGGGCC 2580 GCATTTTATA TTGTAATTAT ATATTTTCAA TTTTGAAATC CCAAAATATT ATCATATTCT 2640 TCCCAATAAA CTCGAGGGTA CCGGATCCTT CTTTATTCTA TACTTAAAAA GTGAAAATAA 2700 ATACAAAGGT TCTTGAGGGT TGTGTTAAAT TGAAAGCGAG AAATAATCAT AAATTATTTC 2760 ATTATCGCGA TATCCGTTAA GTTTGTATCG TAATGTGCCG CCGCCCGGAT TGCGGCTTCT 2820 CTTTCTCACC TGGACCGGTG GCACTGCTGT GGTGTTGCCT TCTGCTGCCC ATCGTTTCCT 2880 CAGCCACCGT CAGCGTCGCT CCTACCGTCG CCGAGAAAGT TCCCGCGGAG TGCCCCGAAC 2940 TAACGCGTCG ATGCCTGTTG GGTGAGGTGT TTCAGGGTGA CAAGTATGAA AGTTGGCTGC 3000 GCCCGTTGGT GAATGTTACC AGACGCGATG GCCCGCTATC GCAACTTATT CGTTACCGTC 3060 CCGTTACGCC GGAGGCCGCC AACTCCGTGC TGTTGGACGA TGCTTTCCTG GACACTCTGG 3120 CCCTGCTGTA CAACAATCCG GATCAATTGC GGGCCTTGCT GACGCTGTTG AGCTCGGACA 3180 CAGCGCCGCG CTGGATGACG GTGATGCGCG GTTACAGCGA GTGCGGCGAT GGCTCGCCGG 3240 CCGTGTACAC GTGCGTGGAC GACCTGTGCC GCGGCTACGA CCTCACGCGA CTGTCATACG 3300 GGCGCAGCAT CTTCACGGAA CACGTGTTAG GCTTCGAGCT GGTGCCACCG TCTCTCTTTA 3360 ACGTGGTGGT GGCCATACGC AACGAAGCCA CGCGTACCAA CCGCGCCGTG CGTCTGCCCG 3420 TGAGCACCGC TGCCGCGCCC GAGGGCATCA CGCTCTTTTA CGGCCTGTAC AACGCAGTGA 3480 AGGAATTCTG CCTGCGTCAC CAGCTGGACC CGCCGCTGCT ACGCCACCTA GATAAATACT 3540 ACGCCGGACT GCCGCCCGAG CTGAAGCAGA CGCGCGTCAA CCTGCCGGCT CACTCGCGCT 3600 ATGGCCCTCA AGCAGTGGAT GCTCGCTAAT TTTTATAGAT CCCCCGGGAA TCGATTCGCG 3660 ATAGCTGATT AGTTTTTGTT AACAAAAATG TGGGAGAATC TAATTAGTTT TTCTTTACAC 3720 AATTGACGTA CATGAGTCTG AGTTCCTTGT TTTTGCTAAT TATTTCATCC AATTTATTAT 3780 TCTTGACGAT ATCGAGATCT TTTGTATAGG AGTCAGACTT GTATTCAACA TGCTTTTCTA 3840 TAATCATCTT AGTTATTTCG GCATCATCCA ATAGTACATT TTCCAGATTA ACAGAGTAGA 3900 TATTAATGTC GTATTTGAAC AGAGCCTGTA ACATCTCAAT GTCTTTATTA TCTATAGCCA 3960 ATTTAATGTC CGGAATGAAG AGAAGGGAAT TATTGGTGTT TGTCGACGTC ATATAGTCGA 4020 GCAAGAGAAT CATCATATCC ACGTGTCCAT TTTTTATAGT GGTGTGAATA CAACTAAGGA 4080 GAATAGCCAG ATCAAAAGTA GATGGTATTT CTGAAAGAAA GTATGATACA ATACTTACAT 4140 CATTAAGCAT GACGGCATGA TAAAATGAAG TTTTCCATCC AGTTTTCCCA TAGAACATCA 4200 GTCTCCAATT TTTCTTAAAC AGTTTCACCG TTTGCATGTT ACCACTATCA ACCGCATAAT 4260 ACAATGCGGT GTTTCCTTTG TCATCAAATT GTGAATCATC CATTCCACTG AATAGCAAAA 4320 TCTTTACTAT TTTGGTATCT TCTAATGTGG CTGCCTGATG TAATGGAAAT TCATTCTCTA 4380 GAAGATTTTT CAATGCTCCA GCGTTCAACA ACGTACATAC TAGACGCACG TTATTATCAG 4440 CTATTGCATA ATACAAGGCA CTATGTCCAT GGACATCCGC CTTAAATGTA TCTTTACTAG 4500 AGAGAAAGCT TTTCAGCTGC TTAGACTTCC AAGTATTAAT TCGTGACAGA TCCATGTCTG 4560 AAACGAGACG CTAATTAGTG TATATTTTTT CATTTTTTAT AATTTTGTCA TATTGCACCA 4620 GAATTAATAA TATCTCTAAT AGATCTAATT TAATTTAATT TATATAACTT ATTTTTTGAA 4680 TATACTTTTA ATTAACAAAA GAGTTAAGTT ACTCATATGG ACGCCGTCCA GTCTGAACAT 4740 CAATCTTTTT AGCCAGAGAT ATCATAGCCG CTCTTAGAGT TTCAGCGTGA TTTTCCAACC 4800 TAAATAGAAC TTCATCGTTG CGTTTACAAC ACTTTTCTAT TTGTTCAAAC TTTGTTGTTA 4860 CATTAGTAAT CTTTTTTTCC AAATTAGTTA GCCGTTGTTT GAGAGTTTCC TCATTGTCGT 4920 CTTCATCGGC TTTAACAATT GCTTCGCGTT TAGCCTCCTG GCTGTTCTTA TCAGCCTTTG 4980 TAGAAAAAAA TTCAGTTGCT GGAATTGCAA GATCGTCATC TCCGGGGAAA AGAGTTCCGT 5040 CCATTTAAAG CCGCGGGAAT TC 5062 3209 base pairs nucleic acid single linear DNA (genomic) unknown 43 TGAATGTTAA ATGTTATACT TTGGATGAAG CTATAAATAT GCATTGGAAA AATAATCCAT 60 TTAAAGAAAG GATTCAAATA CTACAAAACC TAAGCGATAA TATGTTAACT AAGCTTATTC 120 TTAACGACGC TTTAAATATA CACAAATAAA CATAATTTTT GTATAACCTA ACAAATAACT 180 AAAACATAAA AATAATAAAA GGAAATGTAA TATCGTAATT ATTTTACTCA GGAATGGGGT 240 TAAATATTTA TATCACGTGT ATATCTATAC TGTTATCGTA TACTCTTTAC AATTACTATT 300 ACGAATATGC AAGAGATAAT AAGATTACGT ATTTAAGAGA ATCTTGTCAT GATAATTGGG 360 TACGACATAG TGATAAATGC TATTTCGCAT CGTTACATAA AGTCAGTTGG AAAGATGGAT 420 TTGACAGATG TAACTTAATA GGTGCAAAAA TGTTAAATAA CAGCATTCTA TCGGAAGATA 480 GGATACCAGT TATATTATAC AAAAATCACT GGTTGGATAA AACAGATTCT GCAATATTCG 540 TAAAAGATGA AGATTACTGC GAATTTGTAA ACTATGACAA TAAAAAGCCA TTTATCTCAA 600 CGACATCGTG TAATTCTTCC ATGTTTTATG TATGTGTTTC AGATATTATG AGATTACTAT 660 AAACTTTTTG TATACTTATA TTCCGTAAAC TATATTAATC ATGAAGAAAA TGAAAAAGTA 720 TAGAAGCTGT TCACGAGCGG TTGTTGAAAA CAACAAAATT ATACATTCAA GATGGCTTAC 780 ATGTACGTCT GTGAGGCTAT CATGGATAAT GACAATGCAT CTCTAAATAG GTTTTTGGAC 840 AATGGATTCG ACCCTAACAC GGAATATGGT ACTCTACAAT CTCCTCTTGA AATGGCTGTA 900 ATGTTCAAGA ATACCGAGGC TATAAAAATC TTGATGAGGT ATGGAGCTAA ACCTGTAGTT 960 ACTGAATGCA CAACTTCTTG TCTGCATGAT GCGGTGTTGA GAGACGACTA CAAAATAGTA 1020 AAAGATCTGT TGAAGAATAA CTATGTAAAC AATGTTCTTT ACAGCGGAGG CTTTACTCCT 1080 TTGTGTTTGG CAGCTTACCT TAACAAAGTT AATTTGGTTA AACTTCTATT GGCTCATTCG 1140 GCGGATGTAG ATATTTCAAA CACGGATCGG TTAACTCCTC TACATATAGC CGTATCAAAT 1200 AAAAATTTAA CAATGGTTAA ACTTCTATTG AACAAAGGTG CTGATACTGA CTTGCTGGAT 1260 AACATGGGAC GTACTCCTTT AATGATCGCT GTACAATCTG GAAATATTGA AATATGTAGC 1320 ACACTACTTA AAAAAAATAA AATGTCCAGA ACTGGGAAAA ATTGATCTTG CCAGCTGTAA 1380 TTCATGGTAG AAAAGAAGTG CTCAGGCTAC TTTTCAACAA AGGAGCAGAT GTAAACTACA 1440 TCTTTGAAAG AAATGGAAAA TCATATACTG TTTTGGAATT GATTAAAGAA AGTTACTCTG 1500 AGACACAAAA GAGGTAGCTG AAGTGGTACT CTCAAAATGC AGAACGATGA CTGCGAAGCA 1560 AGAAGTAGAG AAATAACACT TTATGACTTT CTTAGTTGTA GAAAAGATAG AGATATAATG 1620 ATGGTCATAG ATAACTCTGA TATTGCAAGT AAATGCAATA ATAAGTTAGA TTTATTTAAA 1680 AGGATAGTTA AAAATAGAAA AAAAGAGTTA ATTTGTAGGG TTAAAATAAT ACATAAGATC 1740 TTAAAATTTA TAAATACGCA TAATAATAAA AATAGATTAT ACTTATTACC TTCAGAGATA 1800 AAATTTAAGA TATTTACTTA TTTAACTTAT AAAGATCTAA AATGCATAAT TTCTAAATAA 1860 TGAAAAAAAA GTACATCATG AGCAACGCGT TAGTATATTT TACAATGGAG ATTAACGCTC 1920 TATACCGTTC TATGTTTATT GATTCAGATG ATGTTTTAGA AAAGAAAGTT ATTGAATATG 1980 AAAACTTTAA TGAAGATGAA GATGACGACG ATGATTATTG TTGTAAATCT GTTTTAGATG 2040 AAGAAGATGA CGCGCTAAAG TATACTATGG TTACAAAGTA TAAGTCTATA CTACTAATGG 2100 CGACTTGTGC AAGAAGGTAT AGTATAGTGA AAATGTTGTT AGATTATGAT TATGAAAAAC 2160 CAAATAAATC AGATCCATAT CTAAAGGTAT CTCCTTTGCA CATAATTTCA TCTATTCCTA 2220 GTTTAGAATA CTTTTCATTA TATTTGTTTA CAGCTGAAGA CGAAAAAAAT ATATCGATAA 2280 TAGAAGATTA TGTTAACTCT GCTAATAAGA TGAAATTGAA TGAGTCTGTG ATAATAGCTA 2340 TAATCAGAGA AGTTCTAAAA GGAAATAAAA ATCTAACTGA TCAGGATATA AAAACATTGG 2400 CTGATGAAAT CAACAAGGAG GAACTGAATA TAGCTAAACT ATTGTTAGAT AGAGGGGCCA 2460 AAGTAAATTA CAAGGATGTT TACGGTTCTT CAGCTCTCCA TAGAGCTGCT ATTGGTAGGA 2520 AACAGGATAT GATAAAGCTG TTAATCGATC ATGGAGCTGA TGTAAACTCT TTAACTATTG 2580 CTAAAGATAA TCTTATTAAA AAAAAATAAT ATCACGTTTA GTAATATTAA AATATATTAA 2640 TAACTCTATT ACTAATAACT CCAGTGGATA TGAACATAAT ACGAAGTTTA TACATTCTCA 2700 TCAAAATCTT ATTGACATCA AGTTAGATTG TGAAAATGAG ATTATGAAAT TAAGGAATAC 2760 AAAAATAGGA TGTAAGAACT TACTAGAATG TTTTATCAAT AATGATATGA ATACAGTATC 2820 TAGGGCTATA AACAATGAAA CGATTAAAAA TTATAAAAAT CATTTCCCTA TATATAATAC 2880 GCTCATAGAA AAATTCATTT CTGAAAGTAT ACTAAGACAC GAATTATTGG ATGGAGTTAT 2940 AAATTCTTTT CAAGGATTCA ATAATAAATT GCCTTACGAG ATTCAGTACA TTATACTGGA 3000 GAATCTTAAT AACCATGAAC TAAAAAAAAT TTTAGATAAT ATACATTAAA AAGGTAAATA 3060 GATCATCTGT TATTATAAGC AAAGATGCTT GTTGCCAATA ATATACAACA GGTATTTGTT 3120 TTTATTTTTA ACTACATATT TGATGTTCAT TCTCTTTATA TAGTATACAC AGAAAATTCA 3180 TAATCCACTT AGAATTTCTA GTTATCTAG 3209 1483 base pairs nucleic acid single linear DNA (genomic) unknown 44 GGTACGTGAC TAATTAGCTA TAAAAAGGAT CTTAATTAAT TAGTCATCAG GCAGGGCGAG 60 AACGAGACTA TCTGCTCGTT AATTAATTAG GTCGACGGAT CCCCCGGGTT CTTTATTCTA 120 TACTTAAAAA GTGAAAATAA ATACAAAGGT TCTTGAGGGT TGTGTTAAAT TGAAAGCGAG 180 AAATAATCAT AAATTATTTC ATTATCGCGA TATCCGTTAA GTTTGTATCG TAATGGAGGA 240 GCCGCAGTCA GATCCTAGCG TCGAGCCCCC TCTGAGTCAG GAAACATTTT CAGACCTATG 300 GAAACTACTT CCTGAAAACA ACGTTCTGTC CCCCTTGCCG TCCCAAGCAA TGGATGATTT 360 GATGCTGTCC CCGGACGATA TTGAACAATG GTTCACTGAA GACCCAGGTC CAGATGAAGC 420 TCCCAGAATG CCAGAGGCTG CTCCCCGCGT GGCCCCTGGA CCAGCAGCTC CTACACCGGC 480 GGCCCCTGCA CCAGCCCCCT CCTGGCCCCT GTCATCTTCT GTCCCTTCCC AGAAAACCTA 540 CCAGGGCAGC TACGGTTTCC GTCTGGGCTT CTTGCATTCT GGGACAGCCA AGTCTGTGAC 600 TTGCACGTAC TCCCCTGCCC TCAACAAGAT GTTTTGCCAA CTGGCCAAGA CCTGCCCTGT 660 GCAGCTGTGG GTTGATTCCA CACCCCCGCC CGGCACCCGC GTCCGCGCCA TGGCCATCTA 720 CAAGCAGTCA CAGCACATGA CGGAGGTTGT GAGGCGCTGC CCCCACCATG AGCGCTGCTC 780 AGATAGCGAT GGTCTGGCCC CTCCTCAGCA TCTTATCCGA GTGGAAGGAA ATTTGCGTGT 840 GGAGTATTTG GATGACAGAA ACACTTTTCG ACATAGTGTG GTGGTGCCCT ATGAGCCGCC 900 TGAGGTTGGC TCTGACTGTA CCACCATCCA CTACAACTAC ATGTGTAACA GTTCCTGCAT 960 GGGCGGCATG AACCGGAGGC CCATCCTCAC CATCATCACA CTGGAAGACT CCAGTGGTAA 1020 TCTACTGGGA CGGAACAGCT TTGAGGTGCG TGTTTGTGCC TGTCCTGGGA GAGACCGGCG 1080 CACAGAGGAA GAGAATCTCC GCAAGAAAGG GGAGCCTCAC CACGAGCTGC CCCCAGGGAG 1140 CACTAAGCGA GCACTGCCCA ACAACACCAG CTCCTCTCCC CAGCCAAAGA AGAAACCACT 1200 GGATGGAGAA TATTTCACCC TTCAGATCCG TGGGCGTGAG CGCTTCGAGA TGTTCCGAGA 1260 GCTGAATGAG GCCTTGGAAC TCAAGGATGC CCAGGCTGGG AAGGAGCCAG GGGGGAGCAG 1320 GGCTCACTCC AGCCACCTGA AGTCCAAAAA GGGTCAGTCT ACCTCCCGCC ATAAAAAACT 1380 CATGTTCAAG ACAGAAGGGC CTGACTCAGA CTGAACGCGT TTTTATCCCG GGCTCGAGTC 1440 TAGAATCGAT CCCGGGTTTT TATGACTAGT TAATCACGGC CGC 1483 1173 base pairs nucleic acid single linear DNA (genomic) unknown 45 ATGACTGCCA TGGAGGAGTC ACAGTCGGAT ATCAGCCTCG AGCTCCCTCT GAGCCAGGAG 60 ACATTTTCAG GCTTATGGAA ACTACTTCCT CCAGAAGATA TCCTGCCATC ACCTCACTGC 120 ATGGACGATC TGTTGCTGCC CCAGGATGTT GAGGAGTTTT TTGAAGGCCC AAGTGAAGCC 180 CTCCGAGTGT CAGGAGCTCC TGCAGCACAG GACCCTGTCA CCGAGACCCC TGGGCCAGTG 240 GCCCCTGCCC CAGCCACTCC ATGGCCCCTG TCATCTTTTG TCCCTTCTCA AAAAACTTAC 300 CAGGGCAACT ATGGCTTCCA CCTGGGCTTC CTGCAGTCTG GGACAGCCAA GTCTGTTATG 360 TGCACGTACT CTCCTCCCCT CAATAAGCTA TTCTGCCAGC TGGCGAAGAC GTGCCCTGTG 420 CAGTTGTGGG TCAGCGCCAC ACCTCCAGCT GGGAGCCGTG TCCGCGCCAT GGCCATCTAC 480 AAGAAGTCAC AGCACATGAC GGAGGTCGTG AGACGCTGCC CCCACCATGA GCGCTGCTCC 540 GATGGTGATG GCCTGGCTCC TCCCCAGCAT CTTATCCGGG TGGAAGGAAA TTTGTATCCC 600 GAGTATCTGG AAGACAGGCA GACTTTTCGC CACAGCGTGG TGGTACCTTA TGAGCCACCC 660 GAGGCCGGCT CTGAGTATAC CACCATCCAC TACAAGTACA TGTGTAATAG CTCCTGCATG 720 GGGGGCATGA ACCGCCGACC TATCCTTACC ATCATCACAC TGGAAGACTC CAGTGGGAAC 780 CTTCTGGGAC GGGACAGCTT TGAGGTTCGT GTTTGTGCCT GCCCTGGGAG AGACCGCCGT 840 ACAGAAGAAG AAAATTTCCG CAAAAAGGAA GTCCTTTGCC CTGAACTGCC CCCAGGGAGC 900 GCAAAGAGAG CGCTGCCCAC CTGCACAAGC GCCTCTCCCC CGCAAAAGAA AAAACCACTT 960 GATGGAGAGT ATTTCACCCT CAAGATCCGC GGGCGTAAAC GCTTCGAGAT GTTCCGGGAG 1020 CTGAATGAGG CCTTAGAGTT AAAGGATGCC CATGCTACAG AGGAGTCTGG AGACAGCAGG 1080 GCTCACTCCA GCTACCTGAA GACCAAGAAG GGCCAGTCTA CTTCCCGCCA TAAAAAAACA 1140 ATGGTCAAGA AAGTGGGGCC TGACTCAGAC TGA 1173 1182 base pairs nucleic acid single linear DNA (genomic) unknown 46 ATGGAGGAGC CGCAGTCAGA TCCTAGCGTC GAGCCCCCTC TGAGTCAGGA AACATTTTCA 60 GACCTATGGA AACTACTTCC TGAAAACAAC GTTCTGTCCC CCTTGCCGTC CCAAGCAATG 120 GATGATTTGA TGCTGTCCCC GGACGATATT GAACAATGGT TCACTGAAGA CCCAGGTCCA 180 GATGAAGCTC CCAGAATGCC AGAGGCTGCT CCCCGCGTGG CCCCTGCACC AGCAGCTCCT 240 ACACCGGCGG CCCCTGCACC AGCCCCCTCC TGGCCCCTGT CATCTTCTGT CCCTTCCCAG 300 AAAACCTACC AGGGCAGCTA CGGTTTCCGT CTGGGCTTCT TGCATTCTGG GACAGCCAAG 360 TCTGTGACTT GCACGTACTC CCCTGCCCTC AACAAGATGT TTTGCCAACT GGCCAAGACC 420 TGCCCTGTGC AGCTGTGGGT TGATTCCACA CCCCCGCCCG GCACCCGCGT CCGCGCCATG 480 GCCATCTACA AGCAGTCACA GCACATGACG GAGGTTGTGA GGCGCTGCCC CCACCATGAG 540 CGCTGCTCAG ATAGCGATGG TCTGGCCCCT CCTCAGCATC TTATCCGAGT GGAAGGAAAT 600 TTGCGTGTGG AGTATTTGGA TGACAGAAAC ACTTTTCGAC ATAGTGTGGT GGTGCCCTAT 660 GAGCCGCCTG AGGTTGGCTC TGACTGTACC ACCATCCACT ACAACTACAT GTGTAACAGT 720 TCCTGCATGG GCGGCATGAA CCGGAGGCCC ATCCTCACCA TCATCACACT GGAAGACTCC 780 AGTGGTAATC TACTGGGACG GAACAGCTTT GAGGTGCGTG TTTGTGCCTG TCCTGGGAGA 840 GACCGGCGCA CAGAGGAAGA GAATCTCCGC AAGAAAGGGG AGCCTCACCA CGAGCTGCCC 900 CCAGGGAGCA CTAAGCGAGC ACTGCCCAAC AACACCAGCT CCTCTCCCCA GCCAAAGAAG 960 AAACCACTGG ATGGAGAATA TTTCACCCTT CAGATCCGTG GGCGTGAGCG CTTCGAGATG 1020 TTCCGAGAGC TGAATGAGGC CTTGGAACTC AAGGATGCCC AGGCTGGGAA GGAGCCAGGG 1080 GGGAGCAGGG CTCACTCCAG CCACCTGAAG TCCAAAAAGG GTCAGTCTAC CTCCCGCCAT 1140 AAAAAACTCA TGTTCAAGAC AGAAGGGCCT GACTCAGACT GA 1182 2336 base pairs nucleic acid single linear DNA (genomic) unknown 47 TATAAATCTC CTAACGCCGT TCGGGCAGTC ACAGTCTTCG GATCGGACGC CGTGGAACGC 60 AGTTCTCAGC GAAGAAGGAC ACCGCCCGAC TCCAGAAGAC ACCGCTGCCC GAAGAAGAGA 120 AGACTTCATC GGTAAGAGAC CCAGCTTCTC CTCCCCGGAG CTTCGGCCAC GCCGCTCCAC 180 ACCCGGGAAC CGAGGCTTCG GAGCCCGATA CCCGGACAGA AGCTTCTCCC CGGCCGCTCC 240 ACATCAGGGA GCCTTGACCG GCGAGCCTGC TATCCGGGTA GAGACTGTCC TGCGGCCGCT 300 TCAGCAGCTC CACGATCGAC GACTGTGACC GTTGAGCCCG CCGTTTAGGC AGAGGCTCCG 360 CTTCAACTAC CCTACCGACA CATTCGCGGT TCTTCCTCCA GAACATCTTA CCCTCTACTC 420 GGCCACTCTA CAAGGACCGG TAATGGATCC AACTCTTTTC ACACAATCAA GACTTCTCAG 480 AGTGAATGAT TATGATGAAG TGCGTGAGTC GGTAAATCAA CCGAGACAGG AACAGCAGCC 540 AGGAGACAGG TGCCCTAGAC ATGTGGCAAG AATCATTGCC GAGAACGATC CTCCAATCAG 600 ATGTGACCTG ACTCTCCAAG AGCTATTGAG TGAGGTGCAG GTGGATTTCG AACCATCGGC 660 ATCAGAGGTC GTGGCAATGG AAGGCCTGAT GGACGAACAA CACTTCATTC CACATGATCC 720 ACATTCTAAA AAAGCAGCCG TTCAAAGTCT TGTAATTGCC ATCAAGACCG CGGACCTCCT 780 GTTGCAAATG ATACATGAGA ATGTTAAAAG AGACATCCGC ACGACATGCA TCCAAATGGC 840 TAATGAATCT TATGCACGTG CGGACATAGT CAGAGATTCA CTGATAGCAG CATCGCAAGG 900 AAAATACACA GCACTCGGGA AAATAGTATT CCACTCCTAT ACAAATTTCA TGCCAGTGAA 960 TGCAAATGAG TCCGAAAAGA GAGCATGGAT GGAAATGCTA GGCGAGTGTA CCAGCCATGG 1020 AAACAAGCTG TGTGAGATGG CAAATGCGCA AGTAGAGCAG GAGACGCGCG ATATAATCAA 1080 TATAATGTTC AAAAATATAG ATGATGTAGT CACACAAACA ACAAGAGCAA TGAGAGGCGT 1140 GTTCGATCCA CCTGACACAG TTAAAGCTCT CTCTGCCGCA GCCCAACTGA TCAGAGTATG 1200 GGAACATGAT AACGTTATAA ATGACCAAAG TGTGTCAACA TCTTCTGTCG TAACGGCTGC 1260 ATTGGAGGCT AACGAGAATT TGGCAAAGGC ACTTAGAGAT GTGTCAGGGT ACGCTGAGGT 1320 GCAATTTAAC AGATTATGCC TTTCTATACT AACATCGGCA AAGGAACGAA TAGACATAAT 1380 CTATCATTCG GCAAGGTCCC AACACCTCGC GTGCAATGTC AGGATGAACG TGGCACAACA 1440 AAACCTAGCA ACTTTCATCC TAACGAATGC CAGAGAGAGG CCAAATGATG CTGTGATCAG 1500 AACACGCAGA GCAGTTGCAA ATACAGGTAT ACTGCTGTTC ACAGGACAAC ATATCACAAG 1560 AGATGCTTTA GATAAAGCTG CAGAGTCAAA AAGTGTAGAA GAAATTGTAG GGATGTCAGT 1620 ACAGGCTAGA CAAGCGCTAG TTGAACAAGA TATGCCTCCA CTAGAGGGAG AAGGTGAGGA 1680 AGCTAGAGAG GAACATGCCG GAGAAGGACA GGCTAGAGAA GGACAGGCCG AAGAAGAACA 1740 GGCCGGAGAA TCTGCGGGAG ATGAGTCCGA AGATGAAGAT GGCGAAGGAA CAAGGTCTCT 1800 GGTCCGTGTG ATCAACATTC CACTCGCGCA ACCTCAGCCG ATAGTGGCGC ACGAGCCTCC 1860 ACCTCAGCCC CAAGAATCGG ATGACAGCGA TACCGAATCT GATGGCGAAG ATCCAATCGC 1920 TAGGCAACAG AATCCCACAC CAACACAAGA GAGCGAACCC ATAACCGAAG ATCCTGAAGA 1980 CTGGCCGGAC GCTCAGAGAC TGATAGAAGA GGAATCTAGC CAAGAAACAC CCCAAGAACC 2040 GGCATCTGAG CAAGAACCAT CCACACCAGG TCCACGCACT AGGAGACGCT CACACCCCCC 2100 AACTGAAGGT TCAGCACCCA AGAGAGGCAG GAGATCATAA GGTGCCAACC AATATCAAAC 2160 CGATCGGGGT ACCAATCATA TAAATCATAA ATGCCAGGAT ACCAATCACA TAATCATATC 2220 AATATGCATC AATAAAATTT TATAATCATA CTCAGAGGGA ACTGCCCACC CTCAATTACC 2280 TATTGATTTT ACAATATATA ATGTAACTGC AATTAATAAA GTACACATGT ACATGA 2336 2115 base pairs nucleic acid single linear DNA (genomic) unknown 48 TATAAATCTC CTAACGCCGT TCGGGCAGTC ACAGTCTTCG GATCGGACGC CGTGGAACGC 60 AGTTCTCAGC GAAGAAGGAC ACCGCCCGAC TCCAGAAGAC ACCGCTGCCC GAAGAAGAGA 120 AGACTTCATC GGTAAGAGAC CCAGCTTCTC CTCCCCGGAG CTTCGGCCAC GCCGCTCCAC 180 ACCCGGGAAC CGAGGCTTCG GAGCCCGATA CCCGGACAGA AGCTTCTCCC CGGCCGCTCC 240 ACATCAGGGA GCCTTGACCG GCGAGCCTGC TATCCGGGTA GAGACTGTCC TGCGGCCGCT 300 TCAGCAGCTC CACGATCGAC GACTGTGACC GTTGAGCCCG CCGTTTAGGC AGAGGCTCCG 360 CTTCAACTAC CCTACCGACA CATTCGCGGT TCTTCCTCCA GAACATCTTA CCCTCTACTC 420 GGCCACTCTA CAAGGACCGG TAATGGATCC AACTCTTTTC ACACAATCAA GACTTCTCAG 480 AGTGAATGAT TATGATGAAG TGCGTGAGTC GGTAAATCAA CCGAGACAGG AACAGCAGCC 540 AGGAGACAGG TGCCCTAGAC ATGTGGCAAG AATCATTGCC GAGAACGATC CTCCAATCAG 600 ATGTGACCTG ACTCTCCAAG AGCTATTGAG TGAGGTGCAG GTGGATTTCG AACCATCGGC 660 ATCAGAGGTC GTGGCAATGG AAGGCCTGAT GGACGAACAA CACTTCATTC CACATGATCC 720 ACATTCTAAA AAAGCAGCCG GGCCTAACGT GAGGCATATA GACATTGTTA CCGCAGCCGC 780 GTCGATGTCA GGGATATCCG GATCAACAGA GAGACCATTA GATGATGGAC AGAGACCCTT 840 AGCTGATGGA TGTTATAGCA AGAAACATAA GAAGCAGAAA CACAGCGAAC CTATAGACAC 900 CAAGGTGCAC ATCCAACGGG GGGAGGAAAC AGACTCTGAT TCAGACTCAG ACACCGGTAA 960 ATCACCGGGA TGCGATGAAA TATCTTTTTA CTTGTCCAGT GCTTCGGATG ATGAACATGG 1020 CAATGGGAAT CGTTCTGGGT TAGAAGGAAA TTGTAGTTCA TATACTTCAC ATTCATCACG 1080 TAGATCAAAA TCGCCGCTAA GAAGTCCTTC AAACAGGCCC CAAAAGAGAA AATTATGTAA 1140 GAATATGTTT ATTACAAAAA GCAAACGTAG GGTAATATGT GAATCTGATT CAGATACAGA 1200 CTCCGAAATC GAGACCAGGC CATTTATCAG ACCACAAGAA CCTCCCAGAC AAAAGAATAA 1260 GGGGAAAAGA TGTCCCAAGA AACATAGAAA GATAAAAGAG CTCATGGATG GGCCAGGATT 1320 CGTGGCTCCG AATGCACACA AACGAGGTAA AAATAGAAAT GAGGGAAACA ACGATGGACG 1380 AGGGAAACCG ACCACACGAG CTTTAGAATA CAAACAGATG CCATACAAAC AGCAAACGGT 1440 CCAGTTTCTC TATGGAAATG CGATAAGGAC ATGTAGAGAG AGCACCGTAC ACGATAAAAT 1500 TATTATGGTG ATGTTTACAC GGGGTCAAGA TATCAGGCAG GCCATAGAAA AGTTGAGATC 1560 CCAACTTGGT CAAATAACCA ACCTTTCCAT ATCTGCTCCC TTCAACACAG AACACACAAA 1620 ACCACAGATA CACACACCAA ACACGGTTAA CATGACATCG CAGGCACTTG CGGCAGGTCT 1680 TCAAGCCTCC TGGAACCTAG ACGAGGATAA TAAACACAAT AATGCACCTA GGATGTCAGA 1740 TTACAGAACC ATGATAATCC AAGCGGCAAC ACCACCAGAT TTTCTAGGTG CACTCAAACT 1800 ATGCATACAG TTCGCACAAA CCTTTCCCAA GAATGCGTGT ATAAGGTTAT GTAATATAGT 1860 TGGAGGCCTA CAACCCCTTC CCATCTACGA AAAAGTCGTC ACCGCTTACA CTGACACGCA 1920 ATATAACTTT AGCCCAATCA CTAACAAAGA TAGTAACGGT GGTATGAGCA CAATATTGGA 1980 TCAGGACTCC GATTCAGAAT AATGAAGAAA CTATCATATT AAATCGTGTA CATATTTTAT 2040 TAAACACTAT TTCCAACCAT GAGACGAGGC TTGTTGATGC AGCTGCTGTT CCTTGGAATA 2100 AATGTAATAT ACTGT 2115 5275 base pairs nucleic acid single linear DNA (genomic) unknown 49 AAGCTTGCGG CCGCTCATTA GACAAGCGAA TGAGGGACGA AAACGTGGAG GAGGTATTAA 60 GTTTGGAGAA ATGGAGAGAG ACTGTTTAAT AGCGCATGGC GCAGCCAATA CTATTACAGA 120 AGTTTTGAAA GATTCGGAAG AAGATTATCA AGATGTGTAT GTTTGTGAAA ATTGTGGAGA 180 CATAGCAGCA CAAATCAAGG GTATTAATAC ATGTCTTAGA TGTTCAAAAC TTAATCTCTC 240 TCCTCTCTTA ACAAAAATTG ATACCACGCA CGTATCTAAA GTATTTCTTA CTCAAATGAA 300 CGCCAGAGGC GTAAAAGTCA AATTAGATTT CGAACGAAGG CCTCCTTCGT TTTATAAACC 360 ATTAGATAAA GTTGATCTCA AGCCGTCTTT TCTGGTGTAA TAAAAATTAA TTAATTACTC 420 GAGATAAAAA TTATGATCTC CTGCCTCTCT TGGGTGCTGA ACCTTCAGTT GGGGGGTGTG 480 AGCGTCTCCT AGTGCGTGGA CCTGGTGTGG ATGGTTCTTG CTCAGATGCC GGTTCTTGGG 540 GTGTTTCTTG GCTAGATTCC TCTTCTATCA GTCTCTGAGC GTCCGGCCAG TCTTCAGGAT 600 CTTCGGTTAT GGGTTCGCTC TCTTGTGTTG GTGTGGGATT CTGTTGCCTA GCGATTGGAT 660 CTTCGCCATC AGATTCGGTA TCGCTGTCAT CCGATTCTTG GGGCTGAGGT GGAGGCTCGT 720 GCGCCACTAT CGGCTGAGGT TGCGCGAGTG GAATGTTGAT CACACGGACC AGAGACCTTC 780 TTCCTTCGCC ATCTTCATCT TCGGACTCAT CTCCCGCAGA TTCTCCGGCC TGTTCTTCTT 840 CGGCCTGTCC TTCTCTAGCC TGTCCTTCTC CGGCATGTTC CTCTCTAGCT TCCTCACCTT 900 CTCCCTCTAG TGGAGGCATA TCTTGTTCAA CTAGCGCTTG TCTAGCCTGT ACTGACATCC 960 CTACAATTTC TTCTACACTT TTTGACTCTG CAGCTTTATC TAAAGCATCT CTTGTGATAT 1020 GTTGTCCTGT GAACAGCAGT ATACCTGTAT TTGCAACTGC TCTGCGTGTT CTGATCACAG 1080 CATCATTTGG CCTCTCTCTG GCATTCGTTA GGATGAAAGT TGCTAGGTTT TGTTGTGCCA 1140 CGTTCATCCT GACATTGCAC GCGAGGTGTT GGGACCTTGC CGAATGATAG ATTATGTCTA 1200 TTCGTTCCTT TGCCGATGTT AGTATAGAAA GGCATAATCT GTTAAATTGC ACCTCAGCGT 1260 ACCCTGACAC ATCTCTAAGT GCCTTTGCCA AATTCTCGTT AGCCTCCAAT GCAGCCGTTA 1320 CGACAGAAGA TGTTGACACA CTTTGGTCAT TTATAACGTT ATCATGTTCC CATACTCTGA 1380 TCAGTTGGGC TGCGGCAGAG AGAGCTTTAA CTGTGTCAGG TGGATCGAAC ACGCCTCTCA 1440 TTGCTCTTGT TGTTTGTGTG ACTACATCAT CTATATTTTT GAACATTATA TTGATTATAT 1500 CGCGCGTCTC CTGCTCTACT TGCGCATTTG CCATCTCACA CAGCTTGTTT CCATGGCTGG 1560 TACACTCGCC TAGCATTTCC ATCCATGCTC TCTTTTCGGA CTCATTTGCA TTCACTGGCA 1620 TGAAATTTGT ATAGGAGTGG AATACTATTT TCCCGAGTGC TGTGTATTTT CCTTGCGATG 1680 CTGCTATCAG TGAATCTCTG ACTATGTCCG CACGTGCATA AGATTCATTA GCCATTTGGA 1740 TGCATGTCGT GCGGATGTCT CTTTTAACAT TCTCATGTAT CATTTGCAAC AGGAGGTCCG 1800 CGGTCTTGAT GGCAATTACA AGACTTTGAA CGGCTGCTTT TTTAGAATGT GGATCATGTG 1860 GAATGAAGTG TTGTTCGTCC ATCAGGCCTT CCATTGCCAC GACCTCTGAT GCCGATGGTT 1920 CGAAATCCAC CTGCACCTCA CTCAATAGCT CTTGGAGAGT CAGGTCACAT CTGATTGGAG 1980 GATCGTTCTC GGCAATGATT CTTGCCACAT GTCTAGGGCA CCTGTCTCCT GGCTGCTGTT 2040 CCTGTCTCGG TTGATTTACC GACTCACGCA CTTCATCATA ATCATTCACT CTGAGAAGTC 2100 TTGATTGTGT GAAAAGAGTT GGATCCATTA CGATACAAAC TTAACGGATA TCGCGATAAT 2160 GAAATAATTT ATGATTATTT CTCGCTTTCA ATTTAACACA ACCCTCAAGA ACCTTTGTAT 2220 TTATTTTCAC TTTTTAAGTA TAGAATAAAG AAGAATTGGG TTTTGGGATT TCAAAATTGA 2280 AAATATATAA TTACAATATA AAATGGATCC AACTCTTTTC ACACAATCAA GACTTCTCAG 2340 AGTGAATGAT TATGATGAAG TGCGTGAGTC GGTAAATCAA CCGAGACAGG AACAGCAGCC 2400 AGGAGACAGG TGCCCTAGAC ATGTGGCAAG AATCATTGCC GAGAACGATC CTCCAATCAG 2460 ATGTGACCTG ACTCTCCAAG AGCTATTGAG TGAGGTGCAG GTGGATTTCG AACCATCGGC 2520 ATCAGAGGTC GTGGCAATGG AAGGCCTGAT GGACGAACAA CACTTCATTC CACATGATCC 2580 ACATTCTAAA AAAGCAGCCG GGCCTAACGT GAGGCATATA GACATTGTTA CCGCAGCCGC 2640 GTCGATGTCA GGGATATCCG GATCAACAGA GAGACCATTA GATGATGGAC AGAGACCCTT 2700 AGCTGATGGA TGTTATAGCA AGAAACATAA GAAGCAGAAA CACAGCGAAC CTATAGACAC 2760 CAAGGTGCAC ATCCAACGGG GGGAGGAAAC AGACTCTGAT TCAGACTCAG ACACCGGTAA 2820 ATCACCGGGA TGCGATGAAA TATCTTTTTA CTTGTCCAGT GCTTCGGATG ATGAACATGG 2880 CAATGGGAAT CGTTCTGGGT TAGAAGGAAA TTGTAGTTCA TATACTTCAC ATTCATCACG 2940 TAGATCAAAA TCGCCGCTAA GAAGTCCTTC AAACAGGCCC CAAAAGAGAA AATTATGTAA 3000 GAATATGTTT ATTACAAAAA GCAAACGTAG GGTAATATGT GAATCTGATT CAGATACAGA 3060 CTCCGAAATC GAGACCAGGC CATTTATCAG ACCACAAGAA CCTCCCAGAC AAAAGAATAA 3120 GGGGAAAAGA CGTCCCAAGA AACATAGAAA GATAACAGAG CTCATGGATG GGCCAGGATT 3180 CGTGGCTCCG AATGCACACA AACGAGGTAA AAATAGAAAT GAGGGAAACA ACGATGGACG 3240 AGGGAAACCG ACCACACGAG CTTTAGAATA CAAACAGATG CCATACAAAC AGCAAACGGT 3300 CCAGTTTCTC TATGGAAATG CGATAAGGAC ATGTAGAGAG AGCACCGTAC ACGATAAAAT 3360 TATTATGGTG ATGTTTACAC GGGGTCAAGA TATCAGGCAG GCCATAGAAA AGTTGAGATC 3420 CCAACTTGGT CAAATAACCA ACCTTTCCAT ATCTGCTCCC TTCAACACAG AACACACAAA 3480 ACCACAGATA CACACACCAA ACACGGTTAA CATGACATCG CAGGCACTTG CGGCAGGTCT 3540 TCAAGCCTCC TGGAACCTAG ACGAGGATAA TAAACACAAT AATGCACCTA GGATGTCAGA 3600 TTACAGAACC ATGATAATCC AAGCGGCAAC ACCACCAGAT TTTCTAGGTG CACTCAAACT 3660 ATGCATACAG TTCGCACAAA CCTTTCCCAA GAATGCGTGT ATAAGGTTAT GTAATATAGT 3720 TGGAGGCCTA CAACCCCTTC CCATCTACGA AAAAGTCGTC ACCGCTTACA CTGACACGCA 3780 ATATAACTTT AGCCCAATCA CTAACAAAGA TAGTAACGGT GGTATGAGCA CAATATTGGA 3840 TCAGGACTCC GATTCAGAAT AATTTTTATC GCGATAGCTG ATTAGTTTTT GTTAACAAAA 3900 ATGTGGGAGA ATCTAATTAG TTTTTCTTTA CACAATTGAC GTACATGAGT CTGAGTTCCT 3960 TGTTTTTGCT AATTATTTCA TCCAATTTAT TATTCTTGAC GATATCGAGA TCTTTTGTAT 4020 AGGAGTCAGA CTTGTATTCA ACATGCTTTT CTATAATCAT CTTAGTTATT TCGGCATCAT 4080 CCAATAGTAC ATTTTCCAGA TTAACAGAGT AGATATTAAT GTCGTATTTG AACAGAGCCT 4140 GTAACATCTC AATGTCTTTA TTATCTATAG CCAATTTAAT GTCCGGAATG AAGAGAAGGG 4200 AATTATTGGT GTTTGTCGAC GTCATATAGT CGAGCAAGAG AATCATCATA TCCACGTGTC 4260 CATTTTTTAT AGTGGTGTGA ATACAACTAA GGAGAATAGC CAGATCAAAA GTAGATGGTA 4320 TTTCTGAAAG AAAGTATGAT ACAATACTTA CATCATTAAG CATGACGGCA TGATAAAATG 4380 AAGTTTTCCA TCCAGTTTTC CCATAGAACA TCAGTCTCCA ATTTTTCTTA AACAGTTTCA 4440 CCGTTTGCAT GTTACCACTA TCAACCGCAT AATACAATGC GGTGTTTCCT TTGTCATCAA 4500 ATTGTGAATC ATCCATTCCA CTGAATAGCA AAATCTTTAC TATTTTGGTA TCTTCTAATG 4560 TGGCTGCCTG ATGTAATGGA AATTCATTCT CTAGAAGATT TTTCAATGCT CCAGCGTTCA 4620 ACAACGTACA TACTAGACGC ACGTTATTAT CAGCTATTGC ATAATACAAG GCACTATGTC 4680 CATGGACATC CGCCTTAAAT GTATCTTTAC TAGAGAGAAA GCTTTTCAGC TGCTTAGACT 4740 TCCAAGTATT AATTCGTGAC AGATCCATGT CTGAAACGAG ACGCTAATTA GTGTATATTT 4800 TTTCATTTTT TATAATTTTG TCATATTGCA CCAGAATTAA TAATATCTCT AATAGATCTA 4860 ATTTAATTTA ATTTATATAA CTTATTTTTT GAATATACTT TTAATTAACA AAAGAGTTAA 4920 GTTACTCATA TGGACGCCGT CCAGTCTGAA CATCAATCTT TTTAGCCAGA GATATCATAG 4980 CCGCTCTTAG AGTTTCAGCG TGATTTTCCA ACCTAAATAG AACTTCATCG TTGCGTTTAC 5040 AACACTTTTC TATTTGTTCA AACTTTCTTG TTACATTAGT AATCTTTTTT TCCAAATTAG 5100 TTAGCCGTTG TTTGAGAGTT TCCTCATTGT CGTCTTCATC GGCTTTAACA ATTGCTTCGC 5160 GTTTAGCCTC CTGGCTGTTC TTATCAGCCT TTGTAGAAAA AAATTCAGTT GCTGGAATTG 5220 CAAGATCGTC ATCTCCGGGG AAAAGAGTTC CGTCCATTTA AAGCCGCGGG AATTC 5275 1740 base pairs nucleic acid single linear DNA (genomic) unknown 50 ATGGAGTCCT CTGCCAAGAG AAAGATGGAC CCTGATAATC CTGACGAGGG CCCTTCCTCC 60 AAGGTGCCAC GGCCCGAGAC ACCCGTGACC AAGGCCACGA CGTTCCTGCA GACTATGTTG 120 AGGAAGGAGG TTAACAGTCA GCTGAGTCTG GGAGACCCGC TGTTTCCAGA GTTGGCCGAA 180 GAATCCCTCA AAACTTTTGA ACAAGTGACC GAGGATTGCA ACGAGAACCC CGAGAAAGAT 240 GTCCTGGCAG AACTCGGTGA CATCCTCGCC CAGGCTGTCA ATCATGCCGG TATCGATTCC 300 AGTAGCACCG GCCCCACGCT GACAACCCAC TTCCGCAGCG TTAGACGCGC CCCTCTTAAC 360 AAGCCGACCC CCACCAGCGT CGCGGTTACT AACACTCCTC TCCCCGGGGC ATCCGCTACT 420 CCCGAGCTCA GCCCGCGTAA GAAACCGCGC AAAACCACGC GTCCTTTCAA GGTGATTATT 480 AAACCGCCCG TGCCTCCCGC GCCTATCATG CTGCCCCTCA TCAAACAGGA AGACATCAAG 540 CCCGAGCCCG ACTTTACCAT CCAGTACCGC AACAAGATTA TCGATACCGC CGGCTGTATC 600 GTGATCTCTG ATAGCGAGGA AGAACAGGGT GAAGAAGTCG AAACCCGCGG TGCTACCGCG 660 TCTTCCCCTT CCACCGGCAG CGGCACGCCG CGAGTGACCT CTCCCACGCA CCCGCTCTCC 720 CAGATGAACC ACCCTCCTCT TCCCGATCCC TTGGGCCGGC CCGATGAAGA TAGTTCCTCT 780 TCGTCTTCCT CCTGCAGTTC GGCTTCGGAC TCGGAGAGTG AGTCCGAGGA GATGAAATGC 840 AGCAGTGGCG GAGGAGCATC CGTGACCTCG AGCCACCATG GGCGCGGCGG TTTTGGTGGC 900 GCGGCCTCCT CCTCTCTGCT GAGCTGCGGC CATCAGAGCA GCGGCGGGGC GAGCACCGGA 960 CCCCGCAAGA AGAAGAGCAA ACGCATCTCC GAGTTGGACA ACGAGAAGGT GCGCAATATC 1020 ATGAAAGATA AGAACACCCC CTTCTGCACA CCCAACGTGC AGACTCGGCG GGGTCGCGTC 1080 AAGATTGACG AGGTGAGCCG CATGTTCCGC AACACCAATC GCTCTCTTGA GTACAAGAAC 1140 CTGCCCTTCA CGATTCCCAG TATGCACCAG GTGTTAGATG AGGCCATCAA AGCCTGCAAA 1200 ACCATGCAGG TGAACAACAA GGGCATCCAG ATTATCTACA CCCGCAATCA TGAGGTGAAG 1260 AGTGAGGTGG ATGCGGTGCG GTGTCGCCTG GGCACCATGT GCAACCTGGC CCTCTCCACT 1320 CCCTTCCTCA TGGAGCACAC CATGCCCGTG ACACATCCAC CCAAAGTGGC GCAGCGCACA 1380 GCCGATGCTT GTAACGAAGG CGTCAAGGCC GCGTGGAGCC TCAAAGAATT GCACACCCAC 1440 CAATTATGCC CCCGTTCCTC CGATTACCGC AACATGATCA TCCACGCTGC CACCCCCGTG 1500 GACCTGTTGG GCGCTCTCAA CCTGTGCCTG CCCCTGATGC AAAAGTTTCC CAAACAGGTC 1560 ATGGTGCGCA TCTTCTCCAC CAACCAGGGT GGGTTCATGC TGCCTATCTA CGAGACGGCC 1620 ACGAAGGCCT ACGCCGTGGG GCAGTTTGAG CAGCCCACCG AGACCCCTCC CGAAGACCTG 1680 GACACCCTGA GCCTGGCCAT CGAGGCAGCC ATCCAGGACC TGAGGAACAA GTCTCAGTAA 1740 56 base pairs nucleic acid single linear DNA (genomic) unknown 51 GCCTCATCGC TGCTGGATAT CCGTTAAGTT TGTATCGTAA TGGAATCCAG GATCTG 56 40 base pairs nucleic acid single linear DNA (genomic) unknown 52 GACAGAGACT TGTGATTTTT ATAAGCTTCG TAAGCTGTCA 40 55 base pairs nucleic acid single linear DNA (genomic) unknown 53 AGCTTCTTTA TTCTATACTT AAAAAGTGAA AATAAATACA AAGGTTCTTG AGGGT 55 73 base pairs nucleic acid single linear DNA (genomic) unknown 54 TGTGTTAAAT TGAAAGCGAG AAATAATCAT AAATTATTTC ATTATCGCGA TATCCGTTAA 60 GTTTGTATCG TAC 73 56 base pairs nucleic acid single linear DNA (genomic) unknown 55 TTATTAGTAT TTAATAAAGT AATAGCGCTA TAGGCAATTC AAACATAGCA TGAGCT 56 72 base pairs nucleic acid single linear DNA (genomic) unknown 56 AGAAATAAGA TATGAATTTT TCACTTTTAT TTATGTTTCC AAGAACTCCC AACACAATTT 60 AACTTTCGCT CT 72 14 base pairs nucleic acid single linear DNA (genomic) unknown 57 GGTCGACGGA TCCT 14 22 base pairs nucleic acid single linear DNA (genomic) unknown 58 GATCAGGATC CGTCGACCTG CA 22 29 base pairs nucleic acid single linear DNA (genomic) unknown 59 CAGTTGGTAC CACTGGTATT TTATTTCAG 29 61 base pairs nucleic acid single linear DNA (genomic) unknown 60 TATCTGAATT CCTGCAGCCC GGGTTTTTAT AGCTAATTAG TCAAATGTGA GTTAATATTA 60 G 61 66 base pairs nucleic acid single linear DNA (genomic) unknown 61 TCGCTGAATT CGATATCAAG CTTATCGATT TTTATGACTA GTTAATCAAA TAAAAAGCAT 60 ACAAGC 66 30 base pairs nucleic acid single linear DNA (genomic) unknown 62 TTATCGAGCT CTGTAACATC AGTATCTAAC 30 37 base pairs nucleic acid single linear DNA (genomic) unknown 63 TCCGGTACCG CGGCCGCAGA TATTTGTTAG CTTCTGC 37 33 base pairs nucleic acid single linear DNA (genomic) unknown 64 TCGCTCGAGT AGGATACCTA CCTACTACCT ACG 33 29 base pairs nucleic acid single linear DNA (genomic) unknown 65 TCGCTCGAGC TTTCTTGACA ATAACATAG 29 30 base pairs nucleic acid single linear DNA (genomic) unknown 66 TAGGAGCTCT TTATACTACT GGGTTACAAC 30 17 base pairs nucleic acid single linear DNA (genomic) unknown 67 AATTCCTCGA GGGATCC 17 15 base pairs nucleic acid single linear DNA (genomic) unknown 68 CGGGATCCCT CGAGG 15 39 base pairs nucleic acid single linear DNA (genomic) unknown 69 TCGGGATCCG GGTTAATTAA TTAGTTATTA GACAAGGTG 39 41 base pairs nucleic acid single linear DNA (genomic) unknown 70 TAGGAATTCC TCGAGTACGA TACAAACTTA AGCGGATATC G 41 45 base pairs nucleic acid single linear DNA (genomic) unknown 71 GGGCTGAAGC TTGCTGGCCG CTCATTAGAC AAGCGAATGA GGGAC 45 62 base pairs nucleic acid single linear DNA (genomic) unknown 72 AGATCTCCCG GGCTCGAGTA ATTAATTAAT TTTTATTACA CCAGAAAAGA CGGCTTGAGA 60 TC 62 64 base pairs nucleic acid single linear DNA (genomic) unknown 73 TAATTACTCG AGCCCGGGAG ATCTAATTTA ATTTAATTTA TATAACTCAT TTTTTGAATA 60 TACT 64 46 base pairs nucleic acid single linear DNA (genomic) unknown 74 TATCTCGAAT TCCCGCGGCT TTAAATGGAC GGAACTCTTT TCCCCC 46 62 base pairs nucleic acid single linear DNA (genomic) unknown 75 GATCTTTTGT TAACAAAAAC TAATCAGCTA TCGCGAATCG ATTCCCGGGG GATCCGGTAC 60 CC 62 62 base pairs nucleic acid single linear DNA (genomic) unknown 76 TCGAGGGTAC CGGATCCCCC GGGAATCGAT TCGCGATAGC TGATTAGTTT TTGTTAACAA 60 AA 62 46 base pairs nucleic acid single linear DNA (genomic) unknown 77 GATCCATGGA CTCGACAGCG GCGTCTCTGC ATGCAGCCGC TGCAGA 46 46 base pairs nucleic acid single linear DNA (genomic) unknown 78 AGCTTCTGCA GCGGCTGCAT GCAGAGACGC CGCTGTCGAG TCCATG 46 33 base pairs nucleic acid single linear DNA (genomic) unknown 79 TACGAATTCT GCAGTTCACC TATGACACGT TGC 33 37 base pairs nucleic acid single linear DNA (genomic) unknown 80 ATAGGATCCA TGGTCGTCCA GACCCTTGAG GTAGGGC 37 48 base pairs nucleic acid single linear DNA (genomic) unknown 81 GCCCTACCTC AAGGGTCTGG ACGACACTCG ACAGCGGCGT CTCTGCAT 48 12 base pairs nucleic acid single linear DNA (genomic) unknown 82 AATTGGTGAC CG 12 12 base pairs nucleic acid single linear DNA (genomic) unknown 83 GATCCGGTCA CC 12 20 base pairs nucleic acid single linear DNA (genomic) unknown 84 TGAAAGACCG AATTCTGCGT 20 25 base pairs nucleic acid single linear DNA (genomic) unknown 85 TGCGATTCAT CGGTTTGTTG TAGAT 25 20 base pairs nucleic acid single linear DNA (genomic) unknown 86 GACCCTTGAG GTAGGGCGGC 20 39 base pairs nucleic acid single linear DNA (genomic) unknown 87 ACTCATAATA GAACCATAAG ATCTACAGAT GGCAACAAT 39 29 base pairs nucleic acid single linear DNA (genomic) unknown 88 CCGAAGCTTT CAGCATGTCT TGAGCATGC 29 29 base pairs nucleic acid single linear DNA (genomic) unknown 89 CTCAAGACAT GCTGATTTTT ATCTCGAGA 29 37 base pairs nucleic acid single linear DNA (genomic) unknown 90 AGCTTCTCGA GATAAAAATC AGCATGTCTT GAGCATG 37 46 base pairs nucleic acid single linear DNA (genomic) unknown 91 AATTCTCGAG TTTATTGGGA AGAATATGAT AATATTTTGG GATTTC 46 42 base pairs nucleic acid single linear DNA (genomic) unknown 92 AAAATTGAAA ATATATAATT ACAATATAAA ATGCGGCCCG GG 42 34 base pairs nucleic acid single linear DNA (genomic) unknown 93 GATCCCCGGG CCGCATTTTA TATTGTAATT ATAT 34 54 base pairs nucleic acid single linear DNA (genomic) unknown 94 ATTTTCAATT TTGAAATCCC AAAATATTAT CATATTCTTC CCAATAAACT CGAG 54 35 base pairs nucleic acid single linear DNA (genomic) unknown 95 TTAGAATTCC CCGGGCTCCC CTCCTACCTC ATCGT 35 34 base pairs nucleic acid single linear DNA (genomic) unknown 96 TTACTGCAGT AAGTGTTAAG TCTCTGTTGG TATC 34 66 base pairs nucleic acid single linear DNA (genomic) unknown 97 AGAAAAATCA GTTAGCTAAG ATCTCCCGGG CTCGAGGGTA CCGGATCCTG ATTAGTTAAT 60 TTTTGT 66 70 base pairs nucleic acid single linear DNA (genomic) unknown 98 GATCACAAAA ATTAACTAAT CAGGATCCGG TACCCTCGAG CCCGGGAGAT CTTAGCTAAC 60 TGATTTTTCT 70 35 base pairs nucleic acid single linear DNA (genomic) unknown 99 ATCATCGAAT TCTGAATGTT AAATGTTATA CTTTG 35 28 base pairs nucleic acid single linear DNA (genomic) unknown 100 GGGGGTACCT TTGAGAGTAC CACTTCAG 28 44 base pairs nucleic acid single linear DNA (genomic) unknown 101 GGGTCTAGAG CGGCCGCTTA TAAAGATCTA AAATGCATAA TTTC 44 35 base pairs nucleic acid single linear DNA (genomic) unknown 102 ATCATCCTGC AGGTATTCTA AACTAGGAAT AGATG 35 82 base pairs nucleic acid single linear DNA (genomic) unknown 103 GTACGTGACT AATTAGCTAT AAAAAGGATC CGGTACCCTC GAGTCTAGAA TCGATCCCGG 60 GTTTTTATGA CTAGTTAATC AC 82 82 base pairs nucleic acid single linear DNA (genomic) unknown 104 GGCCGTGATT AACTAGTCAT AAAAACCCGG GATCGATTCT AGACTCGAGG GTACCGGATC 60 CTTTTTATAG CTAATTAGTC AC 82 70 base pairs nucleic acid single linear DNA (genomic) unknown 105 GATCTTAATT AATTAGTCAT CAGGCAGGGC GAGAACGAGA CTATCTGCTC GTTAATTAAT 60 TAGGTCGACG 70 70 base pairs nucleic acid single linear DNA (genomic) unknown 106 GATCCGTCGA CCTAATTAAT TAACGAGCAG ATAGTCTCGT TCTCGCCCTG CCTGATGACT 60 AATTAATTAA 70 12 base pairs nucleic acid single linear DNA (genomic) unknown 107 AATTGCGGCC GC 12 78 base pairs nucleic acid single linear DNA (genomic) unknown 108 ATAAAAATTA GCTACTCAGG TACCCTGCAG TCGCGAGGAT CCGAATTCCC CGGGCTCGAG 60 TGATTAATTA GTTTTTAT 78 78 base pairs nucleic acid single linear DNA (genomic) unknown 109 ATAAAAACTA ATTAATCACT CGAGCCCGGG GAATTCGGAT CCTCGCGACT GCAGGGTACC 60 TGAGTAGCTA ATTTTTAT 78 35 base pairs nucleic acid single linear DNA (genomic) unknown 110 ACGGATCCAT AAAAATTACT GGTCAGCCTT GCTTC 35 42 base pairs nucleic acid single linear DNA (genomic) unknown 111 ATCCGTTAAG TTTGTATCGT AATGGAGTCC TCTGCCAAGA GA 42 44 base pairs nucleic acid single linear DNA (genomic) unknown 112 CGCGAATTCT CGCGATATCC GTTAAGTTTG TATCGTAATG GAGT 44 30 base pairs nucleic acid single linear DNA (genomic) unknown 113 GCCTCTAGAG TTAACCTCCT TCCTCAACAT 30 29 base pairs nucleic acid single linear DNA (genomic) unknown 114 CGGTCTAGAG GTTATCAGTG TAATGAAGC 29 46 base pairs nucleic acid single linear DNA (genomic) unknown 115 CCGAAGCTTC TCGAGATAAA AATTACTGGT CAGCCTTGCT TCTAGT 46 43 base pairs nucleic acid single linear DNA (genomic) unknown 116 CGATATCCGT TAAGTTTGTA TCGTAATCTG CAGCCCGGGG GGG 43 44 base pairs nucleic acid single linear DNA (genomic) unknown 117 GATCCCCCGG GCTGCAGATT ACGATACAAA CTTAACGGAT ATCG 44 60 base pairs nucleic acid single linear DNA (genomic) unknown 118 CGCGAATTCT CGCGATATCC GTTAAGTTTG TATCGTAATG AAACAGATTA AGGTTCGAGT 60 27 base pairs nucleic acid single linear DNA (genomic) unknown 119 GCCTCTAGAT GCCGCCATGG CCTGACT 27 39 base pairs nucleic acid single linear DNA (genomic) unknown 120 TCGGGATCCG GGTTAATTAA TTAGTCATCA GGCAGGGCG 39 40 base pairs nucleic acid single linear DNA (genomic) unknown 121 TAGCTCGAGG GTACCTACGA TACAAACTTA ACGGATATCG 40 27 base pairs nucleic acid single linear DNA (genomic) unknown 122 TCGGGATCCT TCTTTATTCT ATACTTA 27 72 base pairs nucleic acid single linear DNA (genomic) unknown 123 AATTCTCGCG ATATCCGTTA AGTTTGTATC GTAATGACGA CGTTCCTGCA GACTATGTTG 60 AGGAAGGAGG TT 72 68 base pairs nucleic acid single linear DNA (genomic) unknown 124 AACCTCCTTC CTCAACATAG TCTGCAGGAA CGTCGTCATT ACGATACAAA CTTAACGGAT 60 ATCGCGAG 68 39 base pairs nucleic acid single linear DNA (genomic) unknown 125 CCCCCCGAAT TCGTCGACGA TTGTTCATGA TGGCAAGAT 39 68 base pairs nucleic acid single linear DNA (genomic) unknown 126 CCCGGGGGAT CCCTCGAGGG TACCAAGCTT AATTAATTAA ATATTAGTAT AAAAAGTGAT 60 TTATTTTT 68 77 base pairs nucleic acid single linear DNA (genomic) unknown 127 AAGCTTGGTA CCCTCGAGGG ATCCCCCGGG TAGCTAGCTA ATTTTTCTTT TACGTATTAT 60 ATATGTAATA AACGTTC 77 39 base pairs nucleic acid single linear DNA (genomic) unknown 128 TTTTTTCTGC AGGTAAGTAT TTTTAAAACT TCTAACACC 39 62 base pairs nucleic acid single linear DNA (genomic) unknown 129 GATTATCGCG ATATCCGTTA AGTTTGTATC GTAATGGCAT CCGTACTGGG TCCCATTTCG 60 GG 62 47 base pairs nucleic acid single linear DNA (genomic) unknown 130 GCATAGGTAC CGGATCCATA AAAATCAACC TCGGTGCTTT TTGGGCG 47 29 base pairs nucleic acid single linear DNA (genomic) unknown 131 TAGTTCGGAT CCCCGCTCAG TCGCCTACA 29 29 base pairs nucleic acid single linear DNA (genomic) unknown 132 ATCAAGGGAT CCATCGAAAA AGAAGAGCG 29 61 base pairs nucleic acid single linear DNA (genomic) unknown 133 GATTATCGCG ATATCCGTTA AGTTTGTATC GTAATGGAGT CGCGCGGTCG CCGTTGTCCC 60 G 61 17 base pairs nucleic acid single linear DNA (genomic) unknown 134 ACCTGCATCT TGGTTGC 17 42 base pairs nucleic acid single linear DNA (genomic) unknown 135 ATCATCGAGC TCGCGGCCGC CTATCAAAAG TCTTAATGAG TT 42 72 base pairs nucleic acid single linear DNA (genomic) unknown 136 GAATTCCTCG AGCTGCAGCC CGGGTTTTTA TAGCTAATTA GTCATTTTTT CGTAAGTAAG 60 TATTTTATTT AA 72 72 base pairs nucleic acid single linear DNA (genomic) unknown 137 CCCGGGCTGC AGCTCGAGGA ATTCTTTTTA TTGATTAACT AGTCAAATGA GTATATATAA 60 TTGAAAAAGT AA 72 45 base pairs nucleic acid single linear DNA (genomic) unknown 138 GATGATGGTA CCTTCATAAA TACAAGTTTG ATTAAACTTA AGTTG 45 26 base pairs nucleic acid single linear DNA (genomic) unknown 139 TTCGGATCCG GTTCTGGAGA AAAGCC 26 32 base pairs nucleic acid single linear DNA (genomic) unknown 140 GCTTCCAAGC TTTCCTGAAG GGATTGTAAG CC 32 28 base pairs nucleic acid single linear DNA (genomic) unknown 141 TTCGGATCCG GCTTTCAGTC TCGTCTCC 28 30 base pairs nucleic acid single linear DNA (genomic) unknown 142 TTCGGATCCA TGCAATTGCC CGCGGACAAC 30 99 base pairs nucleic acid single linear DNA (genomic) unknown 143 TTCGAATTCG CTAGCTTTAT TGGGAAGAAT ATGATAATAT TTTGGGATTT CAAAATTGAA 60 AATATATAAT TACAATATAA AATGAGTTTG CAGTTTATC 99 28 base pairs nucleic acid single linear DNA (genomic) unknown 144 TTCTCTAGAT GAGCTCGTTG AACAGCAC 28 44 base pairs nucleic acid single linear DNA (genomic) unknown 145 CCGAAGCTTG CTAGCAATAA AAACTATTCC TCCGTGTTCT TAAT 44 28 base pairs nucleic acid single linear DNA (genomic) unknown 146 GCCTCTAGAT ACGTAAAGCT AAGTTATC 28 30 base pairs nucleic acid single linear DNA (genomic) unknown 147 GCCTCTAGAA TGTGCCGCCG CCCGGATTGC 30 33 base pairs nucleic acid single linear DNA (genomic) unknown 148 CGCAAGCTTA GCGAGCATCC ACTGCTTGAG GGC 33 54 base pairs nucleic acid single linear DNA (genomic) unknown 149 TCCAAGCTTA GATCTATAAA AATTAGCGAG CATCCACTGC TTGAGGGCCA TAGC 54 32 base pairs nucleic acid single linear DNA (genomic) unknown 150 GCCTCTAGAT GCTGACGCTG TTGAGCTCGG AC 32 58 base pairs nucleic acid single linear DNA (genomic) unknown 151 CGCGAATTCT CGCGATATCC GTTAAGTTTG TATCGTAATG TGCCGCCGCC CGGATTGC 58 34 base pairs nucleic acid single linear DNA (genomic) unknown 152 GCCTCTAGAT TCCAGCGCGG CGCTGTGTCC GAGC 34 20 base pairs nucleic acid single linear DNA (genomic) unknown 153 GTACATAAGC TTTTTGCATG 20 70 base pairs nucleic acid single linear DNA (genomic) unknown 154 TATGAATTCC TCGAGGGATC CAGGCCTTTT TTATTGACTA GTTAATCAGT CTAATATACG 60 TACTAAATAC 70 20 base pairs nucleic acid single linear DNA (genomic) unknown 155 CTAATTTCGA ATGTCCGACG 20 66 base pairs nucleic acid single linear DNA (genomic) unknown 156 TTAGAATTCT CGCGACCCGG GTTTTTATAG CTAATTAGTA CTTATTACAA ATACTATAAT 60 ATTTAG 66 35 base pairs nucleic acid single linear DNA (genomic) unknown 157 AATTCGTCGA CGGATCCCTC GAGGGTACCG CATGC 35 31 base pairs nucleic acid single linear DNA (genomic) unknown 158 GCATGCGGTA CCCTCGAGGG ATCCGTCGAC G 31 52 base pairs nucleic acid single linear DNA (genomic) unknown 159 CCGAAGCTTC TCGAGATAAA AATCAACGAC TGTCGGTAGC GTCCACGACG AC 52 16 base pairs nucleic acid single linear DNA (genomic) unknown 160 TCCACTCCAT GCTAGT 16 41 base pairs nucleic acid single linear DNA (genomic) unknown 161 GATCTGACTG CGGCTCCTCC ATTACGATAC AAACTTAACG G 41 45 base pairs nucleic acid single linear DNA (genomic) unknown 162 GTGGGTAAGG GAATTCGGAT CCCCGGGTTA ATTAATTAGT GATAC 45 34 base pairs nucleic acid single linear DNA (genomic) unknown 163 GTTTGTATCG TAATGGAGGA GCCGCAGTCA GATC 34 57 base pairs nucleic acid single linear DNA (genomic) unknown 164 CATTACGATA CAAACTTAAC GGATATCGCG ACGCGTTCAC ACAGGGCAGG TCTTGGC 57 49 base pairs nucleic acid single linear DNA (genomic) unknown 165 TACTACCTCG AGCCCGGGAT AAAAAACGCG TTCAGTCTGA GTCAGGCCC 49 66 base pairs nucleic acid single linear DNA (genomic) unknown 166 GTGTGAACGC GTCGCGATAT CCGTTAAGTT TGTATCGTAA TGCAGCTGCG TGGGCGTGAG 60 CGCTTC 66 33 base pairs nucleic acid single linear DNA (genomic) unknown 167 ATCATCGGAT CCCCCGGGTT CTTTATTCTA TAC 33 1511 base pairs nucleic acid single linear DNA (genomic) unknown 168 GATTAAAGAA AGTTACTCTG AGACACAAAA GAGGTAGCTG AAGTGGTACT CTCAAAGGTA 60 CCCCCGGGTT AATTAATTAG TCATCAGGCA GGGCGAGAAC GAGACTATCT GCTCGTTAAT 120 TAATTAGGTG ACGGATCCCC GGGTTCTTTA TTCTATACTT AAAAAGTGAA AATAAATACA 180 AAGGTTCTTG AGGGTTGTGT TAAATTGAAA GCGAGAAATA ATCATAAATT ATTTCATTAT 240 CGCGATATCC GTTAAGTTTG TATCGTAATG GAGGAGCCGC AGTCAGATCC TAGCGTCGAG 300 CCCCCTCTGA GTCAGGAAAC ATTTTCAGAC CTATGGAAAC TACTTCCTGA AAACAACGTT 360 CTGTCCCCCT TGCCGTCCCA AGCAATGGAT GATTTGATGC TGTCCCCGGA CGATATTGAA 420 CAATGGTTCA CTGAAGACCC AGGTCCAGAT GAAGCTCCCA GAATGCCAGA GGCTGCTCCC 480 CGCGTGGCCC CTGGACCAGC AGCTCCTACA CCGGCGGCCC CTGCACCAGC CCCCTCCTGG 540 CCCCTGTCAT CTTCTGTCCC TTCCCAGAAA ACCTACCAGG GCAGCTACGG TTTCCGTCTG 600 GGCTTCTTGC ATTCTGGGAC AGCCAAGTCT GTGACTTGCA CGTACTCCCC TGCCCTCAAC 660 AAGATGTTTT GCCAACTGGC CAAGACCTGC CCTGTGCAGC TGTGGGTTGA TTCCACACCC 720 CCGCCCGGCA CCCGCGTCCG CGCCATGGCC ATCTACAAGC AGTCACAGCA CATGACGGAG 780 GTTGTGAGGC GCTGCCCCCA CCATGAGCGC TGCTCAGATA GCGATGGTCT GGCCCCTCCT 840 CAGCATCTTA TCCGAGTGGA AGGAAATTTG CGTGTGGAGT ATTTGGATGA CAGAAACACT 900 TTTCGACATA GTGTGGTGGT GCCCTATGAG CCGCCTGAGG TTGGCTCTGA CTGTACCACC 960 ATCCACTACA ACTACATGTG TAACAGTTCC TGCATGGGCG GCATGAACCG GAGGCCCATC 1020 CTCACCATCA TCACACTGGA AGACTCCAGT GGTAATCTAC TGGGACGGAA CAGCTTTGAG 1080 GTGCGTGTTT GTGCCTGTCC TGGGAGAGAC CGGCGCACAG AGGAAGAGAA TCTCCGCAAG 1140 AAAGGGGAGC CTCACCACGA GCTGCCCCCA GGGAGCACTA AGCGAGCACT GCCCAACAAC 1200 ACCAGCTCCT CTCCCCAGCC AAAGAAGAAA CCACTGGATG GAGAATATTT CACCCTTCAG 1260 ATCCGTGGGC GTGAGCGCTT CGAGATGTTC CGAGAGCTGA ATGAGGCCTT GGAACTCAAG 1320 GATGCCCAGG CTGGGAAGGA GCCAGGGGGG AGCAGGGCTC ACTCCAGCCA CCTGAAGTCC 1380 AAAAAGGGTC AGTCTACCTC CCGCCATAAA AAACTCATGT TCAAGACAGA AGGGCCTGAC 1440 TCAGACTGAA CGCGTTTTTA TCCCGGGCTC GAGTCTAGAA TCGATCCCGG GTTTTTATGA 1500 CTAGTTAATC A 1511 35 base pairs nucleic acid single linear DNA (genomic) unknown 169 ATTATTATTG GATCCTTAAT TAATTAGTGA TACGC 35 35 base pairs nucleic acid single linear DNA (genomic) unknown 170 CTCCTCCATG GCAGTCATTA CGATACAAAC TTAAC 35 38 base pairs nucleic acid single linear DNA (genomic) unknown 171 CGTTAAGTTT GTATCGTAAT GACTGCCATG GAGGAGTC 38 36 base pairs nucleic acid single linear DNA (genomic) unknown 172 TAGTAGTAGT AGTAGCTTCT GGAGGAAGTA GTTTCC 36 39 base pairs nucleic acid single linear DNA (genomic) unknown 173 CAGAAGCTAC TACTACTACT ACCCACCTGC ACAAGCGCC 39 43 base pairs nucleic acid single linear DNA (genomic) unknown 174 AACTACTGTC CCGGGATAAA AATCAGTCTG AGTCAGGCCC CAC 43 20 base pairs nucleic acid single linear DNA (genomic) unknown 175 TAGATAAAGC TGCAGAGTCA 20 36 base pairs nucleic acid single linear DNA (genomic) unknown 176 AGACTCGAGA TAAAAATTAT GATCTCCTGC CTCTCT 36 40 base pairs nucleic acid single linear DNA (genomic) unknown 177 CGCAAGCTTC GCGATAAAAA TTATTCTGAA TCGGAGTCCT 40 21 base pairs nucleic acid single linear DNA (genomic) unknown 178 ATGATAATCC AAGCGGCAAC A 21 68 base pairs nucleic acid single linear DNA (genomic) unknown 179 CTAGAGGATC CATTTTATAT TGTAATTATA TATTTTCAAT TTTGAAATCC CAAAACCCGG 60 GAGATCTG 68 68 base pairs nucleic acid single linear DNA (genomic) unknown 180 AATTCAGATC TCCCGGGTTT TGGGATTTCA AAATTGAAAA TATATAATTA CAATATAAAA 60 TGGATCCT 68 30 base pairs nucleic acid single linear DNA (genomic) unknown 181 ATCCGTTAAG TTTGTATCGT AATGGATCCT 30 34 base pairs nucleic acid single linear DNA (genomic) unknown 182 CTAGAGGATC CATTACGATA CAAACTTAAC GGAT 34 57 base pairs nucleic acid single linear DNA (genomic) unknown 183 GCCTCTAGAC TCGAGCGCCG ACCAGTTCTC CATTACGATA CAAACTTAAC GGATATC 57 27 base pairs nucleic acid single linear DNA (genomic) unknown 184 CGCGAATTCT TCTTTATTCT ATACTTA 27 

What is claimed is:
 1. A composition comprising: an expression system which expresses at least one exogenous epitope of interest of CMV and at least one epitope of interest of p53.
 2. A method of inducing a response against cytomegalovirlis comprising administering to a patient in need of such a response a composition comprising: (I) at least one epitone of interest of CMV and/or an expression system which expresses at least one epitope of interest of CMV: and (II) at least one enitope of interest of p53 and/or an expression system which expresses the at least one enitope of p53.
 3. The method of claim 2 further comprising administering treatment for reducing CMV viral burden and/or for inhibiting smooth muscle cell proliferation.
 4. A method of treating conditions associated with cytomegalovirus comprising administering to a patient in need of such treatment a composition comprising: (I) at least one epitope of interest of CMV and/or an expression system which expresses at least one epitope of interest or CMV; and (II) at least one epitope of interest of p53 and/or an expression system which expresses the at least one epitope of p53.
 5. The method of claim 4 further comprising administering treatment for reducing CMV viral burden and/or for inhibiting smooth muscle cell proliferation.
 6. A method of preventing conditions associated with cytomegalovirus comprising administering to a patient in need of such prevention a composition comprising: (I) at least one epitope of interest of CMV and/or an expression system which expresses at least one epitope of interest of CMV; and (II) at least one epitope of interest of p53 and/or an expression system which expresses the at least one epitope of p53.
 7. The method of claim 6, further comprising administering an agent for reducing CMV viral burden and/or for inhibiting smooth muscle cell proliferation.
 8. The method according to any one of claims 2, 4 or 6 wherein the composition comprises an expression system which expresses at least one enitope of interest of CMV and at least one enitope of interest of p53.
 9. The method of claim 8 further comprising administering an agent for reducing CMV viral burden and/or for inhibiting smooth muscle cell proliferation.
 10. The method according to any one of claims 2, 4 or 6 wherein in the composition, (I) comprises the expression system which expresses at least one epitope of interest of CMV.
 11. The method of claim 10 wherein in the composition, the expression system is an adenovirus, poxvirus or DNA plasmid expression system.
 12. The method according to any one of claims 2, 4 or 6 wherein in the composition, (I) comprises the at least one epitope of interest of CMV.
 13. The method of claim 12 wherein in the composition, the at least one epitope of interest is from expression by at least one recombinant.
 14. The method of claim 13 wherein in the composition, the recombinant is an adenovinis, poxvirus, baculovirus, or DNA plasmid expression system.
 15. The method according to any one of claims 2, 4 or 6 wherein in the composition, (II) comprises the at least one epitope of interest of p53.
 16. The method according to any one of claims 2, 4 or 6 wherein in the composition, the CMV is human CMV.
 17. The method according to any one of claims 2, 4 or 6 wherein in the composition, the CMV epitope of interest is selected from IE1 and/or IE2 or a portion thereof; gB; gB with transmembrane deleted therefrom; gH; gL; pp150; pp65; IE1 with amino acids 2-32 deleted therefrom; IE1 with amino acids 292-319 deleted therefrom; IE1 exon 4 segment; gB and gH; gB and pp65; gB, gH and pp65; gB, gH, pp65 and IE1 exon 4 segment; gB, gH, pp65, pp150, and IE1 exon 4 segment; gB, gH, pp65 and pp150; gB, gH, gL, pp65, pp150 and IE1 exon 4 segment; and gB, gH, gL, pp65 and pp150 ; gp64; or portion of such CMV antigens.
 18. The method of claim 17 wherein in the composition, (II) comprises a p53 epitope of interest.
 19. The method according to any one of claims 2, 4 or 6, wherein in the composition, (II) comprises the expression system that expresses the at least one epitope of interest of p53.
 20. The method of claim 19 wherein in the composition, the CMV is human CMV.
 21. The method of claim 19 wherein in the composition, the CMV epitope of interest is selected from IE1 and/or IE2 or a portion thereof; gB; gB with transmembrane deleted therefrom; gH; gL; pp150; pp65; IE1 with amino acids 2-32 deleted therefrom; IE1 with amino acids 292-319 deleted therefrom; IE1 exon 4 segment; gB and gH; gB and pp65; gB, gII and pp65; gB, gH, pp65 and IE1 exon 4 segment; gB, gH, pp65, pp150, and IE1 exon 4 segment; gB, gH, pp65 and pp150; gB, gH, gL, pp65, pp150 and IE1 exon 4 segment; and gB, gH, gL, pp65 and pp150; gp64; or portion of such CMV antigens.
 22. The method of claim 19 wherein in the composition, (I) comprises the expression system which expresses at least one epitope of interest of CMV. 